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dbVar

Database of genomic structural variation

nsv5927933

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:3,692

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: 310 SVs from 42 studies. See in: genome view

Submitted genomic77,881,824-77,885,515

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5927933	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	77,881,824	77,885,515
nsv5927933	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	78,455,959	78,459,650

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17383279	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17383279	Submitted genomic		NC_000013.11:g.778 81824_77885515del	GRCh38 (hg38)		NC_000013.11	Chr13	77,881,824	77,885,515
nssv17383279	Remapped	Perfect	NC_000013.10:g.784 55959_78459650del	GRCh37.p13	First Pass	NC_000013.10	Chr13	78,455,959	78,459,650

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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