A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1132466



Internal ID15985652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29224554..29276552hg38UCSC Ensembl
Innerchr9:29224552..29276550hg19UCSC Ensembl
Innerchr9:29214552..29266550hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3851999
hg1951999
hg1851999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614058
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)nssv1132466
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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