A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5201654



Internal ID8293389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:7292967..7294379hg38UCSC Ensembl
Outerchr20:7273614..7275026hg19UCSC Ensembl
Outerchr20:7221614..7223026hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg381413
hg191413
hg181413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2485140
Supporting Variants
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)essv5201654
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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