A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1169



Internal ID15544565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:108021499..108055053hg38UCSC Ensembl
Outerchr13:108673847..108707401hg19UCSC Ensembl
Outerchr13:107471848..107505402hg18UCSC Ensembl
Outerchr13:107471848..107505402hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg387402
hg197402
hg187402
hg177402
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1177
Supporting Variants
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)nssv1169
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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