A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2646061



Internal ID8362933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:192137937..192139564hg38UCSC Ensembl
Outerchr3:191855726..191857353hg19UCSC Ensembl
Outerchr3:193338420..193340047hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381628
hg191628
hg181628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5361504
SamplesNA18507
Known GenesFGF12
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)esv2646061
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