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dbVar

Database of genomic structural variation

nsv5900748

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:1,044

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: 152 SVs from 40 studies. See in: genome view

Submitted genomic67,487,225-67,488,268

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5900748	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	67,487,225	67,488,268
nsv5900748	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	68,352,943	68,353,986

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17416212	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17416212	Submitted genomic		NC_000004.12:g.674 87225_67488268del	GRCh38 (hg38)		NC_000004.12	Chr4	67,487,225	67,488,268
nssv17416212	Remapped	Perfect	NC_000004.11:g.683 52943_68353986del	GRCh37.p13	First Pass	NC_000004.11	Chr4	68,352,943	68,353,986

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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