A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176051



Internal ID15874320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:61819450..61910343hg38UCSC Ensembl
Innerchr13:62393583..62484476hg19UCSC Ensembl
Innerchr13:61291584..61382477hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3890894
hg1990894
hg1890894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561870
Supporting Variants
SamplesHGDP00524
Known GenesMIR548AN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176051
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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