A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613729



Internal ID16054452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19173785..19236491hg38UCSC Ensembl
Innerchr9:19173783..19236489hg19UCSC Ensembl
Innerchr9:19163783..19226489hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3862707
hg1962707
hg1862707
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1130783
Samples
Known GenesDENND4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613729
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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