A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585182



Internal ID16372591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:630017..642438hg38UCSC Ensembl
Innerchr20:610661..623082hg19UCSC Ensembl
Innerchr20:558661..571082hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3812422
hg1912422
hg1812422
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv935237
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585182
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