A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1658



Internal ID15546221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:89528147..89562189hg38UCSC Ensembl
Outerchr15:90071378..90105420hg19UCSC Ensembl
Outerchr15:87872382..87906424hg18UCSC Ensembl
Outerchr15:87872382..87906424hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg385398
hg195398
hg185398
hg175398
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7214
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)nsv1658
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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