A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665379



Internal ID9931484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73484107..73486625hg38UCSC Ensembl
Outerchr14:73484070..73486675hg38UCSC Ensembl
Innerchr14:73950812..73953330hg19UCSC Ensembl
Outerchr14:73950775..73953380hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382606
hg192606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5445385
SamplesNA20507
Known GenesHEATR4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665379
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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