A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1180



Internal ID15545743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:109398248..109418853hg38UCSC Ensembl
Outerchr13:110050595..110071200hg19UCSC Ensembl
Outerchr13:108848596..108869201hg18UCSC Ensembl
Outerchr13:108848596..108869201hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3820606
hg1920606
hg1820606
hg1720606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9164
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)nsv1180
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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