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dbVar

Database of genomic structural variation

nsv6051497

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:150

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: 88 SVs from 20 studies. See in: genome view

Submitted genomic44,624,152-44,624,301

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6051497	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	44,624,152	44,624,301
nsv6051497	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	45,127,449	45,127,598

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17628880	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17628880	Submitted genomic		NC_000019.10:g.446 24152_44624301del	GRCh38 (hg38)		NC_000019.10	Chr19	44,624,152	44,624,301
nssv17628880	Remapped	Perfect	NC_000019.9:g.4512 7449_45127598del	GRCh37.p13	First Pass	NC_000019.9	Chr19	45,127,449	45,127,598

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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