A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174735



Internal ID15875837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132900981..133118280hg38UCSC Ensembl
Innerchr10:134714485..134931784hg19UCSC Ensembl
Innerchr10:134564475..134781774hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38217300
hg19217300
hg18217300
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552535
Supporting Variants
SamplesHGDP00743
Known GenesGPR123, LOC399829, TTC40
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174735
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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