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dbVar

Database of genomic structural variation

nsv5944768

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:2,024

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: 293 SVs from 53 studies. See in: genome view

Submitted genomic60,334,536-60,336,559

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5944768	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	60,334,536	60,336,559
nsv5944768	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	58,411,897	58,413,920

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17386797	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17386797	Submitted genomic		NC_000017.11:g.603 34536_60336559del	GRCh38 (hg38)		NC_000017.11	Chr17	60,334,536	60,336,559
nssv17386797	Remapped	Perfect	NC_000017.10:g.584 11897_58413920del	GRCh37.p13	First Pass	NC_000017.10	Chr17	58,411,897	58,413,920

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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