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dbVar

Database of genomic structural variation

nsv5888409

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:376

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: 137 SVs from 34 studies. See in: genome view

Submitted genomic77,885,013-77,885,388

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5888409	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	77,885,013	77,885,388
nsv5888409	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	78,594,730	78,595,105

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17448246	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17448246	Submitted genomic		NC_000006.12:g.778 85013_77885388del	GRCh38 (hg38)		NC_000006.12	Chr6	77,885,013	77,885,388
nssv17448246	Remapped	Perfect	NC_000006.11:g.785 94730_78595105del	GRCh37.p13	First Pass	NC_000006.11	Chr6	78,594,730	78,595,105

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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