A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552553



Internal ID16339962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133111200..133112019hg38UCSC Ensembl
Innerchr10:134924704..134925523hg19UCSC Ensembl
Innerchr10:134774694..134775513hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38820
hg19820
hg18820
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1466n54
Supporting Variantsnssv762073, nssv762064, nssv762083, nssv762070, nssv762060, nssv762089, nssv762088, nssv762057, nssv762066, nssv762076, nssv762058, nssv762090, nssv762054, nssv762065, nssv762061, nssv762052, nssv762048, nssv762055, nssv762081, nssv762047, nssv762082, nssv762071, nssv762086, nssv762067, nssv762077, nssv762050, nssv762051, nssv762080, nssv762063, nssv762062, nssv762084, nssv762059, nssv762085, nssv762072, nssv762049, nssv762078, nssv762087, nssv762074, nssv762056, nssv762075, nssv762079, nssv762053, nssv762068, nssv762069
Samples
Known GenesGPR123
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552553
Frequency
Sample Size17421
Observed Gain37
Observed Loss7
Observed Complex0
Frequencyn/a


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