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dbVar

Database of genomic structural variation

nsv6026113

Organism: Homo sapiens

Study:nstd212 (Wu 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:208,510

Publication(s):Wu 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: 624 SVs from 63 studies. See in: genome view

Submitted genomic86,693,177-86,901,686

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6026113	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	86,693,177	86,901,686
nsv6026113	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	87,236,408	87,444,917

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17603473	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17603473	Submitted genomic		NC_000015.10:g.866 93177_86901686del	GRCh38 (hg38)		NC_000015.10	Chr15	86,693,177	86,901,686
nssv17603473	Remapped	Perfect	NC_000015.9:g.8723 6408_87444917del	GRCh37.p13	First Pass	NC_000015.9	Chr15	87,236,408	87,444,917

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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