A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125994



Internal ID15979180
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 StatusS
Merged Variantsnsv613034
Supporting Variants
Samples
Known GenesKANK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125994
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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