A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8167



Internal ID15535697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:151588671..151599993hg38UCSC Ensembl
Outerchr5:150968232..150979554hg19UCSC Ensembl
Outerchr5:150948425..150959747hg18UCSC Ensembl
Outerchr5:150948425..150959747hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3811323
hg1911323
hg1811323
hg1711323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5068
Supporting Variants
SamplesNA12156
Known Genes
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)nssv8167
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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