A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6587696



Internal ID9255340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57294906..57295500hg38UCSC Ensembl
chr15:57587104..57587698hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665410
Supporting Variants
SamplesNA12156
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6587696
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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