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dbVar

Database of genomic structural variation

nsv5577377

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:50

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: 95 SVs from 23 studies. See in: genome view

Submitted genomic132,349,402-132,349,451

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5577377	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	132,349,402	132,349,451
nsv5577377	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	132,670,541	132,670,590

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17146700	deletion	HG02818	Sequencing	Sequence alignment	3,473

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17146700	Submitted genomic		NC_000006.12:g.132 349402_132349451de lT	GRCh38 (hg38)		NC_000006.12	Chr6	132,349,402	132,349,451
nssv17146700	Remapped	Perfect	NC_000006.11:g.132 670541_132670590de lT	GRCh37.p13	First Pass	NC_000006.11	Chr6	132,670,541	132,670,590

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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