A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5515



Internal ID15543948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:82027632..82072303hg38UCSC Ensembl
Outerchr14:82493976..82538647hg19UCSC Ensembl
Outerchr14:81563729..81608400hg18UCSC Ensembl
Outerchr14:81563729..81608400hg17UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3844672
hg1944672
hg1844672
hg1744672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1377
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)nssv5515
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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