A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552696



Internal ID15993419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133452885..133551641hg38UCSC Ensembl
Innerchr10:135266389..135365145hg19UCSC Ensembl
Innerchr10:135116379..135215135hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3898757
hg1998757
hg1898757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1493n54
Supporting Variantsnssv762929
Samples
Known GenesCYP2E1, SCART1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552696
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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