A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7659



Internal ID15206004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:7512472..7557142hg38UCSC Ensembl
Outerchr11:7533703..7578373hg19UCSC Ensembl
Outerchr11:7490279..7534949hg18UCSC Ensembl
Outerchr11:7490279..7534949hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3844671
hg1944671
hg1844671
hg1744671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8877
SamplesNA12156
Known GenesPPFIBP2
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv7659
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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