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dbVar

Database of genomic structural variation

nsv5564636

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:92

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: 200 SVs from 41 studies. See in: genome view

Submitted genomic176,592,197-176,592,288

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5564636	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	176,592,197	176,592,288
nsv5564636	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	176,019,198	176,019,289

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17120614	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
nssv17120614	Submitted genomic		NC_000005.10:g.176 592197_176592288de lG	GRCh38 (hg38)		NC_000005.10	Chr5	176,592,197	176,592,288
nssv17120614	Remapped	Perfect	NC_000005.9:g.1760 19198_176019289del G	GRCh37.p13	First Pass	NC_000005.9	Chr5	176,019,198	176,019,289

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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