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dbVar

Database of genomic structural variation

nsv6002072

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:65

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: 222 SVs from 35 studies. See in: genome view

Submitted genomic133,657,414-133,657,478

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6002072	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	133,657,414	133,657,478
nsv6002072	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	136,522,536	136,522,600

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17583435	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17583435	Submitted genomic		NC_000009.12:g.133 657414_133657478de l	GRCh38 (hg38)		NC_000009.12	Chr9	133,657,414	133,657,478
nssv17583435	Remapped	Perfect	NC_000009.11:g.136 522536_136522600de l	GRCh37.p13	First Pass	NC_000009.11	Chr9	136,522,536	136,522,600

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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