A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176489



Internal ID15531511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122823630..122859529hg38UCSC Ensembl
Innerchr9:125585909..125621808hg19UCSC Ensembl
Innerchr9:124625730..124661629hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3835900
hg1935900
hg1835900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615270
Supporting Variants
SamplesHGDP01154
Known GenesPDCL, RC3H2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176489
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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