A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5264334



Internal ID8356069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:28861720..28863209hg38UCSC Ensembl
Outerchr14:29330926..29332415hg19UCSC Ensembl
Outerchr14:28400677..28402166hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381490
hg191490
hg181490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2600131
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)essv5264334
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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