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dbVar

Database of genomic structural variation

nsv5651410

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert et al. 2021

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: 367 SVs from 52 studies. See in: genome view

Submitted genomic404,454-404,454

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5651410	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	404,454	404,454
nsv5651410	Remapped	Perfect	GRCh37.p13	Primary Assembly	Second Pass	NC_000017.10	Chr17	254,245	254,245
nsv5651410	Remapped	Perfect	GRCh37.p13	PATCHES	First Pass	NW_003315951.1	Chr17\|NW_0 03315951.1	1,817	1,817

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17087540	insertion	NA24385	Sequencing	Sequence alignment	2,573

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17087540	Submitted genomic		NC_000017.11:g.404 454_404455ins146	GRCh38 (hg38)		NC_000017.11	Chr17	404,454	404,454
nssv17087540	Remapped	Perfect	NW_003315951.1:g.1 817_1818ins146	GRCh37.p13	First Pass	NW_003315951.1	Chr17\|NW_0 03315951.1	1,817	1,817
nssv17087540	Remapped	Perfect	NC_000017.10:g.254 245_254246ins146	GRCh37.p13	Second Pass	NC_000017.10	Chr17	254,245	254,245

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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