A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2566072



Internal ID8629630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:94501460..94502878hg38UCSC Ensembl
Outerchr13:95153714..95155132hg19UCSC Ensembl
Outerchr13:93951715..93953133hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381419
hg191419
hg181419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5162657
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)esv2566072
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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