A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552059



Internal ID15992782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102501602..102627177hg38UCSC Ensembl
Innerchr10:104261359..104386934hg19UCSC Ensembl
Innerchr10:104251349..104376924hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38125576
hg19125576
hg18125576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174571
SamplesHGDP00072
Known GenesACTR1A, SUFU
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552059
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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