A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2452061



Internal ID8168933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:91502949..91504413hg38UCSC Ensembl
Outerchr1:91968506..91969970hg19UCSC Ensembl
Outerchr1:91741094..91742558hg18UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg381465
hg191465
hg181465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5197666
SamplesNA18507
Known GenesCDC7
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)esv2452061
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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