A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563265



Internal ID16003988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113065520..113159539hg38UCSC Ensembl
Innerchr13:113719834..113813853hg19UCSC Ensembl
Innerchr13:112767835..112861854hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3894020
hg1994020
hg1894020
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3426n54
Supporting Variantsnssv820448
Samples
Known GenesF10, F7, MCF2L, PROZ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563265
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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