A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551433



Internal ID16338842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:67805187..67937238hg38UCSC Ensembl
Innerchr10:69564945..69696995hg19UCSC Ensembl
Innerchr10:69234951..69367001hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38132052
hg19132051
hg18132051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv749984
Samples
Known GenesDNAJC12, HERC4, SIRT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551433
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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