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dbVar

Database of genomic structural variation

nsv5895485

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:289

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

Submitted genomic185,632,478-185,632,766

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5895485	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	185,632,478	185,632,766
nsv5895485	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	185,350,266	185,350,554

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17413035	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17413035	Submitted genomic		NC_000003.12:g.185 632478_185632766de l	GRCh38 (hg38)		NC_000003.12	Chr3	185,632,478	185,632,766
nssv17413035	Remapped	Perfect	NC_000003.11:g.185 350266_185350554de l	GRCh37.p13	First Pass	NC_000003.11	Chr3	185,350,266	185,350,554

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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