A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610524



Internal ID16051247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15419198..15568674hg38UCSC Ensembl
Innerchr8:15276707..15426183hg19UCSC Ensembl
Innerchr8:15321078..15470554hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38149477
hg19149477
hg18149477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1106857
Samples
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610524
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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