A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1139190



Internal ID15992376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88534316..88535019hg38UCSC Ensembl
Innerchr9:91149231..91149934hg19UCSC Ensembl
Innerchr9:90339051..90339754hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38704
hg19704
hg18704
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614816
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)nssv1139190
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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