A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562255



Internal ID16349664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70534745..70622329hg38UCSC Ensembl
Innerchr13:71108877..71196461hg19UCSC Ensembl
Innerchr13:70006878..70094462hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3887585
hg1987585
hg1887585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175995
SamplesHGDP01220
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562255
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer