A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5947063



Internal ID8924466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89325133..89325192hg38UCSC Ensembl
Outerchr15:89324976..89325345hg38UCSC Ensembl
Innerchr15:89868364..89868423hg19UCSC Ensembl
Outerchr15:89868207..89868576hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678873
Supporting Variants
SamplesNA19382
Known GenesPOLG
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5947063
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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