A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1131864



Internal ID15985050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24424201..24539634hg38UCSC Ensembl
Innerchr9:24424199..24539632hg19UCSC Ensembl
Innerchr9:24414199..24529632hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38115434
hg19115434
hg18115434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613850
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)nssv1131864
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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