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dbVar

Database of genomic structural variation

nsv5896448

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:1,304

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: 664 SVs from 68 studies. See in: genome view

Submitted genomic189,835,805-189,837,108

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5896448	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	189,835,805	189,837,108
nsv5896448	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	190,756,960	190,758,263

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17423285	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17423285	Submitted genomic		NC_000004.12:g.189 835805_189837108de l	GRCh38 (hg38)		NC_000004.12	Chr4	189,835,805	189,837,108
nssv17423285	Remapped	Perfect	NC_000004.11:g.190 756960_190758263de l	GRCh37.p13	First Pass	NC_000004.11	Chr4	190,756,960	190,758,263

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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