A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128809



Internal ID15981995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15794899..15817121hg38UCSC Ensembl
Innerchr9:15794897..15817119hg19UCSC Ensembl
Innerchr9:15784897..15807119hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3822223
hg1922223
hg1822223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613660
Supporting Variants
Samples
Known GenesCCDC171
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1128809
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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