A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv820450



Internal ID16114406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113079021..113109612hg38UCSC Ensembl
Innerchr13:113733335..113763926hg19UCSC Ensembl
Innerchr13:112781336..112811927hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3830592
hg1930592
hg1830592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563267
Supporting Variants
Samples
Known GenesF7, MCF2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv820450
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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