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dbVar

Database of genomic structural variation

nsv5574634

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:63,213

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: 304 SVs from 46 studies. See in: genome view

Submitted genomic154,475,275-154,538,487

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5574634	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	154,475,275	154,538,487
nsv5574634	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	155,396,427	155,459,639

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17123766	deletion	SAMN01096687	Sequencing	Sequence alignment	1,334

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17123766	Submitted genomic		NC_000004.12:g.154 475275_154538487de lG	GRCh38 (hg38)		NC_000004.12	Chr4	154,475,275	154,538,487
nssv17123766	Remapped	Perfect	NC_000004.11:g.155 396427_155459639de lG	GRCh37.p13	First Pass	NC_000004.11	Chr4	155,396,427	155,459,639

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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