A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv762167



Internal ID16056123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133111304..133114635hg38UCSC Ensembl
Innerchr10:134924808..134928139hg19UCSC Ensembl
Innerchr10:134774798..134778129hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383332
hg193332
hg183332
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552564
Supporting Variants
Samples
Known GenesGPR123
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv762167
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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