A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563013



Internal ID16350422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107817476..107830637hg38UCSC Ensembl
Innerchr13:108469824..108482985hg19UCSC Ensembl
Innerchr13:107267825..107280986hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3813162
hg1913162
hg1813162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148938
SamplesHGDP00964
Known GenesFAM155A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563013
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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