A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678238



Internal ID9944343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59780954..59811650hg38UCSC Ensembl
chr15:60073153..60103849hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3830697
hg1930697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6419464, essv6336933, essv6159678
SamplesHG00189, HG01051, HG00148
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678238
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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