A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv815761



Internal ID16109717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73228534..73782546hg38UCSC Ensembl
Innerchr13:73802671..74356683hg19UCSC Ensembl
Innerchr13:72700672..73254684hg18UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38554013
hg19554013
hg18554013
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562343
Supporting Variants
Samples
Known GenesKLF12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv815761
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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