A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552543



Internal ID16339952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133111093..133112019hg38UCSC Ensembl
Innerchr10:134924597..134925523hg19UCSC Ensembl
Innerchr10:134774587..134775513hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38927
hg19927
hg18927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv761986, nssv761985
Samples
Known GenesGPR123
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552543
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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