A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001474



Internal ID68581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119587809..119596005hg38UCSC Ensembl
chr7:119227863..119236059hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg388197
hg198197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476611
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001474
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.013585


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