A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6514n100



Internal ID19016882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80602341..80680179hg38UCSC Ensembl
chr7:80231657..80309495hg19UCSC Ensembl
chr7:80069593..80147431hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3877839
hg1977839
hg1877839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026688, nsv1020745
Samples
Known GenesCD36
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6514n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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