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dbVar

Database of genomic structural variation

nsv5910789

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:60

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: 180 SVs from 28 studies. See in: genome view

Submitted genomic165,868,504-165,868,563

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5910789	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	165,868,504	165,868,563
nsv5910789	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	166,281,992	166,282,051

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17413171	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17413171	Submitted genomic		NC_000006.12:g.165 868504_165868563de l	GRCh38 (hg38)		NC_000006.12	Chr6	165,868,504	165,868,563
nssv17413171	Remapped	Perfect	NC_000006.11:g.166 281992_166282051de l	GRCh37.p13	First Pass	NC_000006.11	Chr6	166,281,992	166,282,051

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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