A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv270n97



Internal ID22815667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143516258..143728285hg38UCSC Ensembl
chr7:143213351..143425378hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38212028
hg19212028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156739, nsv1156735, nsv1156738, nsv1156736
Samples
Known GenesCTAGE15, EPHA1-AS1, FAM115C
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv270n97
Frequency
Sample Size131
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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