A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1590



Internal ID15546153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:69717840..69749518hg38UCSC Ensembl
Outerchr15:70010179..70041857hg19UCSC Ensembl
Outerchr15:67797233..67828911hg18UCSC Ensembl
Outerchr15:67797233..67828911hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg388065
hg198065
hg188065
hg178065
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4161
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)nsv1590
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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