A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1140616



Internal ID15647116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102996195..103053033hg38UCSC Ensembl
Innerchr9:105758477..105815315hg19UCSC Ensembl
Innerchr9:104798298..104855136hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3856839
hg1956839
hg1856839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615038
Supporting Variants
Samples
Known GenesCYLC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1140616
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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