A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5298327



Internal ID8390062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:111524160..111530691hg38UCSC Ensembl
Outerchr3:111243007..111249538hg19UCSC Ensembl
Outerchr3:112725697..112732228hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg386532
hg196532
hg186532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2466211
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)essv5298327
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