A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1004n100



Internal ID20152620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133432263..133586746hg38UCSC Ensembl
chr10:135245767..135400250hg19UCSC Ensembl
chr10:135095757..135250240hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38154484
hg19154484
hg18154484
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040627, nsv1045575
Samples
Known GenesCYP2E1, SCART1, SPRNP1, SYCE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1004n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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