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dbVar

Database of genomic structural variation

nsv5601004

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:295

Publication(s):Ebert et al. 2021

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: 185 SVs from 59 studies. See in: genome view

Submitted genomic113,174,804-113,175,098

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5601004	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	113,174,804	113,175,098
nsv5601004	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	115,937,084	115,937,378

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17159830	deletion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17159830	Submitted genomic		NC_000009.12:g.113 174804_113175098de lT	GRCh38 (hg38)		NC_000009.12	Chr9	113,174,804	113,175,098
nssv17159830	Remapped	Perfect	NC_000009.11:g.115 937084_115937378de lT	GRCh37.p13	First Pass	NC_000009.11	Chr9	115,937,084	115,937,378

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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