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dbVar

Database of genomic structural variation

nsv6033060

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:80

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: 174 SVs from 36 studies. See in: genome view

Submitted genomic3,235,618-3,235,697

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6033060	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	3,235,618	3,235,697
nsv6033060	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	3,285,618	3,285,697

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17610093	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17610093	Submitted genomic		NC_000016.10:g.323 5618_3235697del	GRCh38 (hg38)		NC_000016.10	Chr16	3,235,618	3,235,697
nssv17610093	Remapped	Perfect	NC_000016.9:g.3285 618_3285697del	GRCh37.p13	First Pass	NC_000016.9	Chr16	3,285,618	3,285,697

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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