A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610554



Internal ID16051277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15554099..15589367hg38UCSC Ensembl
Innerchr8:15411608..15446876hg19UCSC Ensembl
Innerchr8:15455979..15491247hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3835269
hg1935269
hg1835269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1106930
Samples
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610554
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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