A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2612036



Internal ID8675594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:140224010..140225781hg38UCSC Ensembl
Outerchr4:141145164..141146935hg19UCSC Ensembl
Outerchr4:141364614..141366385hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg381772
hg191772
hg181772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5353334
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)esv2612036
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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