A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673742



Internal ID9939847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93103258..93104427hg38UCSC Ensembl
Outerchr15:93103221..93104477hg38UCSC Ensembl
Innerchr15:93646487..93647656hg19UCSC Ensembl
Outerchr15:93646450..93647706hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381257
hg191257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6016438
SamplesNA18870
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673742
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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