A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1159



Internal ID15545722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:103106068..103140053hg38UCSC Ensembl
Outerchr13:103758418..103792403hg19UCSC Ensembl
Outerchr13:102556419..102590404hg18UCSC Ensembl
Outerchr13:102556419..102590404hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg385430
hg195430
hg185430
hg175430
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9159
SamplesNA12156
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)nsv1159
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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