A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674946



Internal ID9941051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69961725..69965874hg38UCSC Ensembl
chr15:70254064..70258213hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg384150
hg194150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5714604, essv6303669, essv5758775, essv5567980, essv5472707
SamplesNA19916, NA18868, NA19707, NA19469, NA19312
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674946
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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