A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561394



Internal ID16348803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:30337394..30377377hg38UCSC Ensembl
Innerchr13:30911531..30951514hg19UCSC Ensembl
Innerchr13:29809531..29849514hg18UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3839984
hg1939984
hg1839984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176348
SamplesHGDP01023
Known GenesLINC00426
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561394
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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