A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5206798



Internal ID8298533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:96415496..96416178hg38UCSC Ensembl
Outerchr10:98175253..98175935hg19UCSC Ensembl
Outerchr10:98165243..98165925hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38499
hg19499
hg18499
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2622954
Supporting Variants
SamplesNA18507
Known GenesTLL2
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)essv5206798
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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