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dbVar

Database of genomic structural variation

nsv5903304

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:928

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: 341 SVs from 55 studies. See in: genome view

Submitted genomic196,329,047-196,329,974

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5903304	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	196,329,047	196,329,974
nsv5903304	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	196,055,918	196,056,845

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17423651	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17423651	Submitted genomic		NC_000003.12:g.196 329047_196329974de l	GRCh38 (hg38)		NC_000003.12	Chr3	196,329,047	196,329,974
nssv17423651	Remapped	Perfect	NC_000003.11:g.196 055918_196056845de l	GRCh37.p13	First Pass	NC_000003.11	Chr3	196,055,918	196,056,845

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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