A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2646380



Internal ID8363252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:62624184..62626824hg38UCSC Ensembl
Outerchr3:62609859..62612499hg19UCSC Ensembl
Outerchr3:62584899..62587539hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg382641
hg192641
hg182641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5173882
SamplesNA18507
Known GenesCADPS
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)esv2646380
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