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dbVar

Database of genomic structural variation

nsv5896366

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:2,406

Publication(s):Almarri et al. 2020

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

Submitted genomic151,759,846-151,762,251

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5896366	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	151,759,846	151,762,251
nsv5896366	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	151,477,634	151,480,039

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17409639	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17409639	Submitted genomic		NC_000003.12:g.151 759846_151762251de l	GRCh38 (hg38)		NC_000003.12	Chr3	151,759,846	151,762,251
nssv17409639	Remapped	Perfect	NC_000003.11:g.151 477634_151480039de l	GRCh37.p13	First Pass	NC_000003.11	Chr3	151,477,634	151,480,039

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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