A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5331159



Internal ID8422894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:90564314..90565825hg38UCSC Ensembl
Outerchr5:89860131..89861642hg19UCSC Ensembl
Outerchr5:89895887..89897398hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381512
hg191512
hg181512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2582955
Supporting Variants
SamplesNA18507
Known GenesGPR98
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)essv5331159
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer