A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2445764



Internal ID8509323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:897845..899545hg38UCSC Ensembl
Outerchr17:801085..802785hg19UCSC Ensembl
Outerchr17:747835..749535hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381701
hg191701
hg181701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5391758
SamplesNA18507
Known GenesNXN
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)esv2445764
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