A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9142



Internal ID15534722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:78705933..78738961hg38UCSC Ensembl
Outerchr13:79280068..79313096hg19UCSC Ensembl
Outerchr13:78178069..78211097hg18UCSC Ensembl
Outerchr13:78178069..78211097hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg386396
hg196396
hg186396
hg176396
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1100
Supporting Variants
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)nssv9142
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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