A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1137726



Internal ID15644226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78148514..78292030hg38UCSC Ensembl
Innerchr9:80763430..80906946hg19UCSC Ensembl
Innerchr9:79953250..80096766hg18UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38143517
hg19143517
hg18143517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614745
Supporting Variants
Samples
Known GenesCEP78
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1137726
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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