A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700182



Internal ID15436834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22821674..22859456hg38UCSC Ensembl
Innerchr11:22843220..22881002hg19UCSC Ensembl
Innerchr11:22799796..22837578hg18UCSC Ensembl
Innerchr11:22799796..22837578hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3837783
hg1937783
hg1837783
hg1737783
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524283
Supporting Variants
Samples
Known GenesCCDC179, SVIP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700182
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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