A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702725



Internal ID15439377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80544432..80571320hg38UCSC Ensembl
Innerchr11:80255476..80282364hg19UCSC Ensembl
Innerchr11:79933124..79960012hg18UCSC Ensembl
Innerchr11:79933124..79960012hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3826889
hg1926889
hg1826889
hg1726889
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526424
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702725
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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