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dbVar

Database of genomic structural variation

nsv5574310

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:70,328

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: 851 SVs from 89 studies. See in: genome view

Submitted genomic25,266,047-25,336,374

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5574310	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	25,266,047	25,336,374
nsv5574310	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	25,592,538	25,662,865

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17064633	deletion	SAMN00006580	Sequencing	Sequence alignment	9,409

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17064633	Submitted genomic		NC_000001.11:g.252 66047_25336374delC	GRCh38 (hg38)		NC_000001.11	Chr1	25,266,047	25,336,374
nssv17064633	Remapped	Perfect	NC_000001.10:g.255 92538_25662865delC	GRCh37.p13	First Pass	NC_000001.10	Chr1	25,592,538	25,662,865

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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