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dbVar

Database of genomic structural variation

nsv6039066

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:58

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: 141 SVs from 33 studies. See in: genome view

Submitted genomic69,325,382-69,325,439

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6039066	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	69,325,382	69,325,439
nsv6039066	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	69,359,285	69,359,342

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17633618	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17633618	Submitted genomic		NC_000016.10:g.693 25382_69325439del	GRCh38 (hg38)		NC_000016.10	Chr16	69,325,382	69,325,439
nssv17633618	Remapped	Perfect	NC_000016.9:g.6935 9285_69359342del	GRCh37.p13	First Pass	NC_000016.9	Chr16	69,359,285	69,359,342

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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