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dbVar

Database of genomic structural variation

nsv5936803

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:145

Publication(s):Almarri et al. 2020

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: 136 SVs from 23 studies. See in: genome view

Submitted genomic76,732,086-76,732,230

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5936803	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	76,732,086	76,732,230
nsv5936803	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	74,728,168	74,728,312

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17377377	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17377377	Submitted genomic		NC_000017.11:g.767 32086_76732230del	GRCh38 (hg38)		NC_000017.11	Chr17	76,732,086	76,732,230
nssv17377377	Remapped	Perfect	NC_000017.10:g.747 28168_74728312del	GRCh37.p13	First Pass	NC_000017.10	Chr17	74,728,168	74,728,312

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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