A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9239



Internal ID15534625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:99029161..99062723hg38UCSC Ensembl
Outerchr14:99495498..99529060hg19UCSC Ensembl
Outerchr14:98565251..98598813hg18UCSC Ensembl
Outerchr14:98565251..98598813hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg385876
hg195876
hg185876
hg175876
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1420
Supporting Variants
SamplesNA12156
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)nssv9239
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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