A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658628



Internal ID9924733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41172823..41173536hg38UCSC Ensembl
Outerchr15:41172786..41173586hg38UCSC Ensembl
Innerchr15:41465021..41465734hg19UCSC Ensembl
Outerchr15:41464984..41465784hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6102183, essv5651012, essv6001791
SamplesHG01462, HG00361, HG01384
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658628
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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