A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2645763



Internal ID8709321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:117281689..117283042hg38UCSC Ensembl
Outerchr10:119041200..119042553hg19UCSC Ensembl
Outerchr10:119031190..119032543hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381354
hg191354
hg181354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5284705
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)esv2645763
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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