A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660232



Internal ID9926337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65326077..65326473hg38UCSC Ensembl
chr15:65618415..65618811hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5887427, essv6153298, essv5557713, essv6088621, essv5669086, essv6334819, essv6346591, essv6231322, essv6224601, essv6250123, essv6415894, essv5428675, essv6590390, essv5674999, essv6030983, essv6443680, essv5449064, essv6380124, essv5561647, essv6434356, essv6152484, essv5999699, essv6357187, essv6069387, essv5746035, essv5463451, essv5863894, essv5574670, essv6189597, essv5422604, essv5545046, essv5663290, essv6442231
SamplesNA20543, NA19664, HG00242, HG01374, NA12058, NA20507, HG00261, NA19660, NA20798, HG00736, HG01365, HG00139, NA06984, NA18868, NA19789, NA20755, NA11831, HG01171, HG00245, NA20521, HG01102, NA11919, NA11894, NA19675, NA19685, HG00136, NA19679, HG00339, HG01491, NA19779, HG00131, NA19900, NA20503
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660232
Frequency
Sample Size1151
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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