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dbVar

Database of genomic structural variation

nsv5587429

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:152

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: 218 SVs from 27 studies. See in: genome view

Submitted genomic35,987,427-35,987,578

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5587429	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	35,987,427	35,987,578
nsv5587429	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	33,567,390	33,567,541

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17100881	deletion	HG03125	Sequencing	Sequence alignment	5,031

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17100881	Submitted genomic		NC_000018.10:g.359 87427_35987578delC	GRCh38 (hg38)		NC_000018.10	Chr18	35,987,427	35,987,578
nssv17100881	Remapped	Perfect	NC_000018.9:g.3356 7390_33567541delC	GRCh37.p13	First Pass	NC_000018.9	Chr18	33,567,390	33,567,541

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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