A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1131404



Internal ID15984590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22739632..22784111hg38UCSC Ensembl
Innerchr9:22739631..22784110hg19UCSC Ensembl
Innerchr9:22729631..22774110hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3844480
hg1944480
hg1844480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613788
Supporting Variants
Samples
Known GenesFLJ35282
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1131404
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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