A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5859486



Internal ID8836889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27158055..27164639hg38UCSC Ensembl
chr15:27403202..27409786hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg386585
hg196585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659305
Supporting Variants
SamplesNA10851
Known GenesGABRG3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5859486
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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