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dbVar

Database of genomic structural variation

nsv6033462

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:184

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: 34 SVs from 12 studies. See in: genome view

Submitted genomic83,241,074-83,241,257

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6033462	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	83,241,074	83,241,257
nsv6033462	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	81,188,843	81,189,026

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17625039	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17625039	Submitted genomic		NC_000017.11:g.832 41074_83241257del	GRCh38 (hg38)		NC_000017.11	Chr17	83,241,074	83,241,257
nssv17625039	Remapped	Perfect	NC_000017.10:g.811 88843_81189026del	GRCh37.p13	First Pass	NC_000017.10	Chr17	81,188,843	81,189,026

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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