A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1131825



Internal ID15985011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23929315..24049509hg38UCSC Ensembl
Innerchr9:23929313..24049507hg19UCSC Ensembl
Innerchr9:23919313..24039507hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38120195
hg19120195
hg18120195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613828
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1131825
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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