A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552724



Internal ID15993447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133535722..133540747hg38UCSC Ensembl
Innerchr10:135349226..135354251hg19UCSC Ensembl
Innerchr10:135199216..135204241hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg385026
hg195026
hg185026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763001
Samples
Known GenesCYP2E1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552724
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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