A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1279



Internal ID15544444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:101152041..101187235hg38UCSC Ensembl
Outerchr15:101692246..101727440hg19UCSC Ensembl
Outerchr15:99509769..99544963hg18UCSC Ensembl
Outerchr15:99509769..99544963hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg385802
hg195802
hg185802
hg175802
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1691
Supporting Variants
SamplesNA19240
Known GenesCHSY1
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)nssv1279
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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