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dbVar

Database of genomic structural variation

nsv6013040

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:166,276

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: 464 SVs from 63 studies. See in: genome view

Submitted genomic120,504,040-120,670,315

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6013040	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	120,504,040	120,670,315
nsv6013040	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	120,144,094	120,310,369

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17561201	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17561201	Submitted genomic		NC_000007.14:g.120 504040_120670315du p	GRCh38 (hg38)		NC_000007.14	Chr7	120,504,040	120,670,315
nssv17561201	Remapped	Perfect	NC_000007.13:g.120 144094_120310369du p	GRCh37.p13	First Pass	NC_000007.13	Chr7	120,144,094	120,310,369

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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