A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6515n100



Internal ID19016883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80626939..80647440hg38UCSC Ensembl
chr7:80256255..80276756hg19UCSC Ensembl
chr7:80094191..80114692hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3820502
hg1920502
hg1820502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027411, nsv1032295, nsv1023254
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)dgv6515n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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