A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4137



Internal ID15538864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:106320549..106355989hg38UCSC Ensembl
Outerchr14:106776806..106811915hg19UCSC Ensembl
Outerchr14:105847851..105882960hg18UCSC Ensembl
Outerchr14:105847851..105882960hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3835441
hg1935110
hg1835110
hg1735110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1443
Supporting Variants
SamplesNA12878
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)nssv4137
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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