A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677592



Internal ID9943697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64041509..64081808hg38UCSC Ensembl
Outerchr16:64041352..64081961hg38UCSC Ensembl
Innerchr16:64075413..64115712hg19UCSC Ensembl
Outerchr16:64075256..64115865hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3840610
hg1940610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6374142, essv5951730
SamplesNA19332, NA19431
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677592
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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