A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6699n100



Internal ID22792786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143506489..143711325hg38UCSC Ensembl
chr7:143203582..143408418hg19UCSC Ensembl
chr7:142913704..143039351hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38204837
hg19204837
hg18125648
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025186, nsv1022170, nsv1026018, nsv1034293, nsv1031935, nsv1024822, nsv1026915, nsv1032078, nsv1020781, nsv1018534, nsv1022293, nsv1031225, nsv1017872, nsv1029477, nsv1017203, nsv1023164, nsv1034640
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)dgv6699n100
Frequency
Sample Size11257
Observed Gain48
Observed Loss0
Observed Complex0
Frequencyn/a


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