A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615039



Internal ID16055762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103001834..103037961hg38UCSC Ensembl
Innerchr9:105764116..105800243hg19UCSC Ensembl
Innerchr9:104803937..104840064hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3836128
hg1936128
hg1836128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140617
Samples
Known GenesCYLC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615039
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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