A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv777156



Internal ID16071112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64329761..64344456hg38UCSC Ensembl
Innerchr11:64097233..64111928hg19UCSC Ensembl
Innerchr11:63853809..63868504hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3814696
hg1914696
hg1814696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555192
Supporting Variants
Samples
Known GenesCCDC88B, MIR7155
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv777156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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