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dbVar

Database of genomic structural variation

nsv5891362

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:1,115

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: 342 SVs from 56 studies. See in: genome view

Submitted genomic196,328,950-196,330,064

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5891362	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	196,328,950	196,330,064
nsv5891362	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	196,055,821	196,056,935

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17418246	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17418246	Submitted genomic		NC_000003.12:g.196 328950_196330064de l	GRCh38 (hg38)		NC_000003.12	Chr3	196,328,950	196,330,064
nssv17418246	Remapped	Perfect	NC_000003.11:g.196 055821_196056935de l	GRCh37.p13	First Pass	NC_000003.11	Chr3	196,055,821	196,056,935

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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