A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8561



Internal ID15188617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:133472514..133517392hg38UCSC Ensembl
Outerchr8:134484757..134529635hg19UCSC Ensembl
Outerchr8:134553939..134598817hg18UCSC Ensembl
Outerchr8:134553939..134598817hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3844879
hg1944879
hg1844879
hg1744879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405
Supporting Variants
SamplesNA12156
Known GenesST3GAL1
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)nssv8561
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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