A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141



Internal ID15199018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:98456199..98488887hg38UCSC Ensembl
Outerchr13:99108453..99141141hg19UCSC Ensembl
Outerchr13:97906454..97939142hg18UCSC Ensembl
Outerchr13:97906454..97939142hg17UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg388304
hg198304
hg188304
hg178304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1164
SamplesNA19240
Known GenesSTK24
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)nsv1141
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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