A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552567



Internal ID16339976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133111410..133112019hg38UCSC Ensembl
Innerchr10:134924914..134925523hg19UCSC Ensembl
Innerchr10:134774904..134775513hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38610
hg19610
hg18610
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv762172, nssv762174, nssv762173
Samples
Known GenesGPR123
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552567
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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