A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128800



Internal ID15981986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15296357..15358159hg38UCSC Ensembl
Innerchr9:15296355..15358157hg19UCSC Ensembl
Innerchr9:15286355..15348157hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3861803
hg1961803
hg1861803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613651
Supporting Variants
Samples
Known GenesTTC39B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1128800
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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