A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1167



Internal ID15545730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:105318159..105351481hg38UCSC Ensembl
Outerchr13:105970510..106003831hg19UCSC Ensembl
Outerchr13:104768511..104801832hg18UCSC Ensembl
Outerchr13:104768511..104801832hg17UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg387634
hg197634
hg187634
hg177634
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1167
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)nsv1167
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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