A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148926



Internal ID15873801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102006303..102066879hg38UCSC Ensembl
Innerchr13:102658653..102719229hg19UCSC Ensembl
Innerchr13:101456654..101517230hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3860577
hg1960577
hg1860577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562977
Supporting Variants
SamplesHGDP00356
Known GenesFGF14, MIR4705
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148926
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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