nsv993395

Organism: Homo sapiens

Study:nstd94 (Helman et al. 2014)
Variant Type:mobile element insertion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:35
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Helman et al. 2014

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 294 SVs from 36 studies. See in: genome view

Remapped(Score: Perfect):26,876,928-26,876,928

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv993395	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nsv993395	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000021.8	Chr21	28,249,247	28,249,247

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv3356073	mobile element insertion	TCGA-21-1076	Sequencing	Split read and paired-end mapping	1,120
nssv3356074	mobile element insertion	TCGA-21-1078	Sequencing	Split read and paired-end mapping	971
nssv3356075	mobile element insertion	TCGA-43-3394	Sequencing	Split read and paired-end mapping	1,043
nssv3356076	mobile element insertion	TCGA-BB-4225	Sequencing	Split read and paired-end mapping	660
nssv3356077	mobile element insertion	TCGA-CR-6482	Sequencing	Split read and paired-end mapping	1,338
nssv3356078	mobile element insertion	TCGA-CR-6487	Sequencing	Split read and paired-end mapping	1,163
nssv3356079	mobile element insertion	TCGA-CV-7100	Sequencing	Split read and paired-end mapping	1,023
nssv3356080	mobile element insertion	TCGA-CV-7416	Sequencing	Split read and paired-end mapping	836
nssv3356081	mobile element insertion	TCGA-CR-6467	Sequencing	Split read and paired-end mapping	1,106
nssv3356082	mobile element insertion	TCGA-CV-5442	Sequencing	Split read and paired-end mapping	1,087
nssv3356083	mobile element insertion	TCGA-A5-A0GG	Sequencing	Split read and paired-end mapping	1,128
nssv3356084	mobile element insertion	TCGA-AP-A05D	Sequencing	Split read and paired-end mapping	993
nssv3356085	mobile element insertion	TCGA-AP-A0L8	Sequencing	Split read and paired-end mapping	1,057
nssv3356086	mobile element insertion	TCGA-D1-A16G	Sequencing	Split read and paired-end mapping	1,092
nssv3356087	mobile element insertion	TCGA-05-4389	Sequencing	Split read and paired-end mapping	579
nssv3356088	mobile element insertion	TCGA-55-6986	Sequencing	Split read and paired-end mapping	1,151
nssv3356089	mobile element insertion	TCGA-67-3771	Sequencing	Split read and paired-end mapping	869
nssv3356090	mobile element insertion	TCGA-06-0744	Sequencing	Split read and paired-end mapping	1,155
nssv3356091	mobile element insertion	TCGA-06-5411	Sequencing	Split read and paired-end mapping	1,080
nssv3356092	mobile element insertion	TCGA-26-5135	Sequencing	Split read and paired-end mapping	1,101
nssv3356093	mobile element insertion	TCGA-AB-2986	Sequencing	Split read and paired-end mapping	488
nssv3356094	mobile element insertion	TCGA-A3-3370	Sequencing	Split read and paired-end mapping	867
nssv3356095	mobile element insertion	TCGA-CZ-5987	Sequencing	Split read and paired-end mapping	1,045
nssv3356096	mobile element insertion	TCGA-13-0723	Sequencing	Split read and paired-end mapping	800
nssv3356097	mobile element insertion	TCGA-AA-A00R	Sequencing	Split read and paired-end mapping	952
nssv3356098	mobile element insertion	TCGA-A2-A0EY	Sequencing	Split read and paired-end mapping	1,047
nssv3356099	mobile element insertion	TCGA-A2-A0YG	Sequencing	Split read and paired-end mapping	922
nssv3356100	mobile element insertion	TCGA-A8-A08S	Sequencing	Split read and paired-end mapping	984
nssv3356101	mobile element insertion	TCGA-AQ-A04J	Sequencing	Split read and paired-end mapping	1,019
nssv3356102	mobile element insertion	TCGA-B6-A0RE	Sequencing	Split read and paired-end mapping	1,003
nssv3356103	mobile element insertion	TCGA-A2-A0D1	Sequencing	Split read and paired-end mapping	1,072
nssv3356104	mobile element insertion	TCGA-A8-A08L	Sequencing	Split read and paired-end mapping	922
nssv3356105	mobile element insertion	TCGA-AO-A03L	Sequencing	Split read and paired-end mapping	1,079
nssv3356106	mobile element insertion	TCGA-AO-A0J2	Sequencing	Split read and paired-end mapping	1,031
nssv3356107	mobile element insertion	TCGA-AR-A0TX	Sequencing	Split read and paired-end mapping	1,128

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv3356073	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356074	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356075	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356076	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356077	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356078	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356079	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356080	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356081	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356082	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356083	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356084	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356085	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356086	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356087	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356088	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356089	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356090	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356091	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356092	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356093	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356094	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356095	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356096	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356097	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356098	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356099	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356100	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356101	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356102	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356103	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356104	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356105	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356106	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356107	Remapped	Perfect	NC_000021.9:g.2687 6928_26876929ins?	GRCh38.p12	First Pass	NC_000021.9	Chr21	26,876,928	26,876,928
nssv3356073	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356074	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356075	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356076	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356077	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356078	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356079	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356080	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356081	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356082	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356083	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356084	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356085	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356086	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356087	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356088	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356089	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356090	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356091	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356092	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356093	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356094	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356095	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356096	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356097	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356098	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356099	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356100	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356101	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356102	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356103	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356104	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356105	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356106	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247
nssv3356107	Submitted genomic		NC_000021.8:g.2824 9247_28249248ins?	GRCh37 (hg19)		NC_000021.8	Chr21	28,249,247	28,249,247

dbVar

Database of genomic structural variation

nsv993395

Links to Other Resources

Genome View

Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant