A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5532



Internal ID15543927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:106326175..106386774hg38UCSC Ensembl
Outerchr14:106782432..106842706hg19UCSC Ensembl
Outerchr14:105853477..105913751hg18UCSC Ensembl
Outerchr14:105853477..105913751hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3860600
hg1960275
hg1860275
hg1760275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
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)nssv5532
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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