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dbVar

Database of genomic structural variation

nsv6041873

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:112

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: 138 SVs from 26 studies. See in: genome view

Submitted genomic38,809,252-38,809,363

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6041873	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	38,809,252	38,809,363
nsv6041873	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	39,299,892	39,300,003

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17627982	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17627982	Submitted genomic		NC_000019.10:g.388 09252_38809363del	GRCh38 (hg38)		NC_000019.10	Chr19	38,809,252	38,809,363
nssv17627982	Remapped	Perfect	NC_000019.9:g.3929 9892_39300003del	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,299,892	39,300,003

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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