Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv5545719

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop et al. 2022)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Byrska-Bishop et al. 2022

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: 99 SVs from 16 studies. See in: genome view

Submitted genomic218,583,717-218,583,717

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5545719	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	218,583,717	218,583,717
nsv5545719	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	219,448,440	219,448,440

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16928243	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16928243	Submitted genomic		NC_000002.12:g.218 583717_218583718in s390	GRCh38 (hg38)		NC_000002.12	Chr2	218,583,717	218,583,717
nssv16928243	Remapped	Perfect	NC_000002.11:g.219 448440_219448441in s390	GRCh37.p13	First Pass	NC_000002.11	Chr2	219,448,440	219,448,440

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16928243	<0.001	2	6398

You are here: NCBI