A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8877



Internal ID15188301
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 StatusS
Merged Variantsnsv7659
Supporting Variants
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)nssv8877
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer