A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615244



Internal ID16055967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114286329..114311308hg38UCSC Ensembl
Innerchr9:117048609..117073588hg19UCSC Ensembl
Innerchr9:116088430..116113409hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3824980
hg1924980
hg1824980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176484
SamplesHGDP00688
Known GenesCOL27A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615244
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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