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dbVar

Database of genomic structural variation

nsv5921713

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:105

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: 139 SVs from 29 studies. See in: genome view

Submitted genomic121,038,135-121,038,239

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5921713	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	121,038,135	121,038,239
nsv5921713	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	120,678,189	120,678,293

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17437012	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17437012	Submitted genomic		NC_000007.14:g.121 038135_121038239de l	GRCh38 (hg38)		NC_000007.14	Chr7	121,038,135	121,038,239
nssv17437012	Remapped	Perfect	NC_000007.13:g.120 678189_120678293de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	120,678,189	120,678,293

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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