A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1160



Internal ID15545723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:103230396..103255723hg38UCSC Ensembl
Outerchr13:103882746..103908073hg19UCSC Ensembl
Outerchr13:102680747..102706074hg18UCSC Ensembl
Outerchr13:102680747..102706074hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3814672
hg1914672
hg1814672
hg1714672
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2051
SamplesNA18555
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)nsv1160
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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