A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037025



Internal ID18779556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133487827..133532494hg38UCSC Ensembl
Innerchr10:135301331..135345998hg19UCSC Ensembl
Innerchr10:135151321..135195988hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3844668
hg1944668
hg1844668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504613
Samples
Known GenesCYP2E1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037025
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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