A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4105



Internal ID15202095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:167723508..167754073hg38UCSC Ensembl
Outerchr3:167441296..167471861hg19UCSC Ensembl
Outerchr3:168923990..168954555hg18UCSC Ensembl
Outerchr3:168923998..168954563hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg389462
hg199462
hg189462
hg179462
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2429
SamplesNA18555
Known GenesPDCD10, SERPINI1
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)nsv4105
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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