A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1494



Internal ID15546057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:36450672..36460695hg38UCSC Ensembl
Outerchr15:36742873..36752896hg19UCSC Ensembl
Outerchr15:34530165..34540188hg18UCSC Ensembl
Outerchr15:34530165..34540188hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg389152
hg199152
hg189152
hg179152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5550
SamplesNA19129
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)nsv1494
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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