A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156436



Internal ID15854446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2353522..2596783hg38UCSC Ensembl
Innerchr9:2353522..2596783hg19UCSC Ensembl
Innerchr9:2343522..2586783hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38243262
hg19243262
hg18243262
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613132
Supporting Variants
Samples1780862125_A
Known GenesFLJ35024
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156436
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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