A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6043593



Internal ID9549065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93222944..93230188hg38UCSC Ensembl
Outerchr15:93222907..93230238hg38UCSC Ensembl
Innerchr15:93766173..93773417hg19UCSC Ensembl
Outerchr15:93766136..93773467hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg387332
hg197332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675292
Supporting Variants
SamplesNA19080
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6043593
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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