A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561700



Internal ID16349109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:54059238..54094377hg38UCSC Ensembl
Innerchr13:54633373..54668512hg19UCSC Ensembl
Innerchr13:53531374..53566513hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3835140
hg1935140
hg1835140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176352
SamplesHGDP01306
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561700
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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