A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2646957



Internal ID8710515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:7096388..7098861hg38UCSC Ensembl
Outerchr20:7077035..7079508hg19UCSC Ensembl
Outerchr20:7025035..7027508hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg382474
hg192474
hg182474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5199285
SamplesNA18507
Known Genes
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)esv2646957
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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