A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1137588



Internal ID15990774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76933238..76942269hg38UCSC Ensembl
Innerchr9:79548154..79557185hg19UCSC Ensembl
Innerchr9:78737974..78747005hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg389032
hg199032
hg189032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614704
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)nssv1137588
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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