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dbVar

Database of genomic structural variation

nsv4768906

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:insertion
Method Type:Curated
Submitted on:GRCh37

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

Description:nsv4684875 from Lee et. al 2020. For a full list of variants now included in nstd186, refer to the mapping file provided here.

Links to Other Resources

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: 124 SVs from 19 studies. See in: genome view

Remapped(Score: Perfect):63,547,434-63,547,434

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4768906	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	63,547,434	63,547,434
nsv4768906	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	61,624,795	61,624,795

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16252983	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16252983	Remapped	Perfect	NC_000017.11:g.635 47434_63547435ins?	GRCh38.p12	First Pass	NC_000017.11	Chr17	63,547,434	63,547,434
nssv16252983	Submitted genomic		NC_000017.10:g.616 24795_61624796ins?	GRCh37 (hg19)		NC_000017.10	Chr17	61,624,795	61,624,795

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16252983	0.111	368	3338

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