A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552056



Internal ID15992779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101441506..101584832hg38UCSC Ensembl
Innerchr10:103201263..103344589hg19UCSC Ensembl
Innerchr10:103191253..103334579hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38143327
hg19143327
hg18143327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv756075
Samples
Known GenesBTRC, POLL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552056
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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