A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664756



Internal ID9584175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42129205..42141617hg38UCSC Ensembl
chr15:42421403..42433815hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3812413
hg1912413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6327544, essv5705592, essv6587765, essv6444806, essv5958520
SamplesNA19066, NA19005, NA19082, NA18952, NA19072
Known GenesPLA2G4F
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664756
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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