A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6297930



Internal ID9275333
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 Flag1
Merged StatusS
Merged Variantsesv2668795
Supporting Variants
SamplesNA18873
Known GenesGABRA5, GABRG3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6297930
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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