A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv762193



Internal ID16056149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133174792..133184562hg38UCSC Ensembl
Innerchr10:134988296..134998066hg19UCSC Ensembl
Innerchr10:134838286..134848056hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg389771
hg199771
hg189771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552577
Supporting Variants
Samples
Known GenesKNDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv762193
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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