A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615037



Internal ID16055760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102993931..103122482hg38UCSC Ensembl
Innerchr9:105756213..105884764hg19UCSC Ensembl
Innerchr9:104796034..104924585hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38128552
hg19128552
hg18128552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140615
Samples
Known GenesCYLC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615037
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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