A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661138



Internal ID9927243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87568651..87573524hg38UCSC Ensembl
Outerchr16:87568614..87573574hg38UCSC Ensembl
Innerchr16:87602257..87607130hg19UCSC Ensembl
Outerchr16:87602220..87607180hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg384961
hg194961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv513e199
Supporting Variantsessv5558483
SamplesNA19070
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661138
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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