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dbVar

Database of genomic structural variation

nsv5571030

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:87

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: 121 SVs from 32 studies. See in: genome view

Submitted genomic87,323,031-87,323,117

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5571030	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	87,323,031	87,323,117
nsv5571030	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	88,032,749	88,032,835

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17144172	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
nssv17144172	Submitted genomic		NC_000006.12:g.873 23031_87323117delT	GRCh38 (hg38)		NC_000006.12	Chr6	87,323,031	87,323,117
nssv17144172	Remapped	Perfect	NC_000006.11:g.880 32749_88032835delT	GRCh37.p13	First Pass	NC_000006.11	Chr6	88,032,749	88,032,835

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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