A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2653755



Internal ID8370627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:145037898..145039460hg38UCSC Ensembl
Outerchr4:145959050..145960612hg19UCSC Ensembl
Outerchr4:146178500..146180062hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg381563
hg191563
hg181563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5348822
SamplesNA18507
Known GenesANAPC10
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)esv2653755
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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