A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5531



Internal ID15543928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105862166..105892940hg38UCSC Ensembl
Outerchr14:106328376..106358798hg19UCSC Ensembl
Outerchr14:105399421..105429843hg18UCSC Ensembl
Outerchr14:105399421..105429843hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3830775
hg1930423
hg1830423
hg1730423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1443
Supporting Variants
SamplesNA19129
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)nssv5531
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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