A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562143



Internal ID16349552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:67551488..67600264hg38UCSC Ensembl
Innerchr13:68125620..68174396hg19UCSC Ensembl
Innerchr13:67023621..67072397hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3848777
hg1948777
hg1848777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175957
SamplesHGDP00603
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562143
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