A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552526



Internal ID15993249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132699017..133103793hg38UCSC Ensembl
Innerchr10:134512521..134917297hg19UCSC Ensembl
Innerchr10:134362511..134767287hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38404777
hg19404777
hg18404777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv761971
Samples
Known GenesGPR123, INPP5A, LOC399829, NKX6-2, TTC40
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552526
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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