A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674549



Internal ID9940654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70735365..70760787hg38UCSC Ensembl
Outerchr15:70735328..70760837hg38UCSC Ensembl
Innerchr15:71027704..71053126hg19UCSC Ensembl
Outerchr15:71027667..71053176hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3825510
hg1925510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5648119
SamplesNA18572
Known GenesUACA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674549
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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