A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2633566



Internal ID8350438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:37913769..37914815hg38UCSC Ensembl
Outerchr20:36542171..36543217hg19UCSC Ensembl
Outerchr20:35975585..35976631hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38267
hg19267
hg18267
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5254575
SamplesNA18507
Known GenesVSTM2L
MethodSequencing
AnalysisLarger insertions and deletions are found by looking at variation in mate pair distances in the 2x50 mate pair libraries. These data are included in separate files for each of three coverage values: 2.2x, 4.0x, 5.6x, and 8.4x
PlatformNot specified
CommentsoriginalFile=Yoruban_large_indels_8.4x.gff
ReferenceMcKernan_et_al_2009
Pubmed ID19546169
Accession Number(s)esv2633566
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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