A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561381



Internal ID16348790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26732414..26748640hg38UCSC Ensembl
Innerchr13:27306551..27322777hg19UCSC Ensembl
Innerchr13:26204551..26220777hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3816227
hg1916227
hg1816227
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3100n54
Supporting Variantsnssv1176343
SamplesHGDP00695
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561381
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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