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dbVar

Database of genomic structural variation

nsv5577351

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:3,605

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: 405 SVs from 71 studies. See in: genome view

Submitted genomic54,063,911-54,067,515

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5577351	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	54,063,911	54,067,515
nsv5577351	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	53,928,709	53,932,313

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17152597	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
nssv17152597	Submitted genomic		NC_000006.12:g.540 63911_54067515delT	GRCh38 (hg38)		NC_000006.12	Chr6	54,063,911	54,067,515
nssv17152597	Remapped	Perfect	NC_000006.11:g.539 28709_53932313delT	GRCh37.p13	First Pass	NC_000006.11	Chr6	53,928,709	53,932,313

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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