A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153695



Internal ID15873237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:42991162..43003012hg38UCSC Ensembl
Innerchr6:42958900..42970750hg19UCSC Ensembl
Innerchr6:43066878..43078728hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3811851
hg1911851
hg1811851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602993
Supporting Variants
SamplesHGDP00148
Known GenesPPP2R5D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153695
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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