A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671800



Internal ID9937905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89058854..89067090hg38UCSC Ensembl
Outerchr15:89058817..89067140hg38UCSC Ensembl
Innerchr15:89602085..89610321hg19UCSC Ensembl
Outerchr15:89602048..89610371hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg388324
hg198324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6296751
SamplesNA12058
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671800
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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