A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1139316



Internal ID15992502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89646949..89675959hg38UCSC Ensembl
Innerchr9:92261864..92290874hg19UCSC Ensembl
Innerchr9:91451684..91480694hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3829011
hg1929011
hg1829011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614850
Supporting Variants
Samples
Known GenesUNQ6494
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1139316
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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