A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1593



Internal ID15546156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:70541657..70577005hg38UCSC Ensembl
Outerchr15:70833996..70869344hg19UCSC Ensembl
Outerchr15:68621050..68656398hg18UCSC Ensembl
Outerchr15:68621050..68656398hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385644
hg195644
hg185644
hg175644
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1259
SamplesNA19240
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)nsv1593
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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