A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5279986



Internal ID8371721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:88939847..88943555hg38UCSC Ensembl
Outerchr15:89483078..89486786hg19UCSC Ensembl
Outerchr15:87284082..87287790hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383709
hg193709
hg183709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2502601
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)essv5279986
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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