A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614216



Internal ID16401625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38066799..38069461hg38UCSC Ensembl
Innerchr9:38066796..38069458hg19UCSC Ensembl
Innerchr9:38056796..38059458hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg382663
hg192663
hg182663
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12674n54
Supporting Variantsnssv1133971
Samples
Known GenesSHB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614216
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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