A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040627



Internal ID18783158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133432263..133561696hg38UCSC Ensembl
Innerchr10:135245767..135375200hg19UCSC Ensembl
Innerchr10:135095757..135225190hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38129434
hg19129434
hg18129434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1004n100
Supporting Variantsnssv3507831
Samples
Known GenesCYP2E1, SCART1, SYCE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040627
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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