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dbVar

Database of genomic structural variation

nsv6022507

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:78

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: 106 SVs from 27 studies. See in: genome view

Submitted genomic23,665,975-23,666,052

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6022507	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	23,665,975	23,666,052
nsv6022507	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	23,677,296	23,677,373

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17614514	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17614514	Submitted genomic		NC_000016.10:g.236 65975_23666052del	GRCh38 (hg38)		NC_000016.10	Chr16	23,665,975	23,666,052
nssv17614514	Remapped	Perfect	NC_000016.9:g.2367 7296_23677373del	GRCh37.p13	First Pass	NC_000016.9	Chr16	23,677,296	23,677,373

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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