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dbVar

Database of genomic structural variation

nsv5922998

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:317

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: 209 SVs from 55 studies. See in: genome view

Submitted genomic139,057,522-139,057,838

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5922998	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	139,057,522	139,057,838
nsv5922998	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	138,742,268	138,742,584

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17441230	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17441230	Submitted genomic		NC_000007.14:g.139 057522_139057838de l	GRCh38 (hg38)		NC_000007.14	Chr7	139,057,522	139,057,838
nssv17441230	Remapped	Perfect	NC_000007.13:g.138 742268_138742584de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	138,742,268	138,742,584

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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