A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6703n100



Internal ID19017071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143519636..143728611hg38UCSC Ensembl
chr7:143216729..143425704hg19UCSC Ensembl
chr7:142926851..143056637hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38208976
hg19208976
hg18129787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024608, nsv1027198, nsv1028666, nsv1026173, nsv1025908, nsv1025732, nsv1029447, nsv1033075, nsv1022867, nsv1031385, nsv1025155
Samples
Known GenesCTAGE15, EPHA1-AS1, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6703n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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