A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668795



Internal ID9588214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26828678..27745183hg38UCSC Ensembl
Outerchr15:26828644..27745218hg38UCSC Ensembl
Innerchr15:27073825..27990329hg19UCSC Ensembl
Outerchr15:27073791..27990364hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38916575
hg19916574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6297930
SamplesNA18873
Known GenesGABRA5, GABRG3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668795
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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