A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1106



Internal ID15545669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:83721082..83756408hg38UCSC Ensembl
Outerchr13:84295217..84330543hg19UCSC Ensembl
Outerchr13:83193218..83228544hg18UCSC Ensembl
Outerchr13:83193218..83228544hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg385650
hg195650
hg185650
hg175650
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156
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)nsv1106
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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