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dbVar

Database of genomic structural variation

nsv5905749

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:137

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: 123 SVs from 32 studies. See in: genome view

Submitted genomic124,628,145-124,628,281

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5905749	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	124,628,145	124,628,281
nsv5905749	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	124,346,992	124,347,128

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17397499	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17397499	Submitted genomic		NC_000003.12:g.124 628145_124628281de l	GRCh38 (hg38)		NC_000003.12	Chr3	124,628,145	124,628,281
nssv17397499	Remapped	Perfect	NC_000003.11:g.124 346992_124347128de l	GRCh37.p13	First Pass	NC_000003.11	Chr3	124,346,992	124,347,128

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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