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dbVar

Database of genomic structural variation

nsv5576844

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:69

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: 370 SVs from 57 studies. See in: genome view

Submitted genomic196,334,893-196,334,961

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5576844	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	196,334,893	196,334,961
nsv5576844	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	196,061,764	196,061,832

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17139307	deletion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17139307	Submitted genomic		NC_000003.12:g.196 334893_196334961de lG	GRCh38 (hg38)		NC_000003.12	Chr3	196,334,893	196,334,961
nssv17139307	Remapped	Perfect	NC_000003.11:g.196 061764_196061832de lG	GRCh37.p13	First Pass	NC_000003.11	Chr3	196,061,764	196,061,832

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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