A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5221084



Internal ID8312819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:46494297..46495628hg38UCSC Ensembl
Outerchr13:47068432..47069763hg19UCSC Ensembl
Outerchr13:45966433..45967764hg18UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg381332
hg191332
hg181332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422736
Supporting Variants
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)essv5221084
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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