A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125995



Internal ID15979181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:613908..704075hg38UCSC Ensembl
Innerchr9:613908..704075hg19UCSC Ensembl
Innerchr9:603908..694075hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3890168
hg1990168
hg1890168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613035
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)nssv1125995
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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