A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613034



Internal ID16400443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:613908..696683hg38UCSC Ensembl
Innerchr9:613908..696683hg19UCSC Ensembl
Innerchr9:603908..686683hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3882776
hg1982776
hg1882776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12458n54
Supporting Variantsnssv1125994
Samples
Known GenesKANK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613034
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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