A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9619



Internal ID15540183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:63152233..63170112hg38UCSC Ensembl
Outerchr3:63137909..63155788hg19UCSC Ensembl
Outerchr3:63112949..63130828hg18UCSC Ensembl
Outerchr3:63112949..63130828hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3814215
hg1914215
hg1814215
hg1714215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3847
Supporting Variants
SamplesNA18507
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)nssv9619
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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