A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676077



Internal ID9942182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27224850..27226643hg38UCSC Ensembl
chr15:27469997..27471790hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381794
hg191794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5987725, essv5685483, essv6106731, essv6026793
SamplesNA19190, NA19338, NA20296, HG01061
Known GenesGABRG3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676077
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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