A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1139759



Internal ID15992945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:98099105..98114002hg38UCSC Ensembl
Innerchr9:100861387..100876284hg19UCSC Ensembl
Innerchr9:99901208..99916105hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3814898
hg1914898
hg1814898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614935
Supporting Variants
Samples
Known GenesTRIM14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1139759
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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