A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5987725



Internal ID9625297
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 Flag1
Merged StatusS
Merged Variantsesv2676077
Supporting Variants
SamplesNA19338
Known GenesGABRG3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5987725
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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