A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586485



Internal ID16373894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62306724..62312525hg38UCSC Ensembl
Innerchr20:60881780..60887581hg19UCSC Ensembl
Innerchr20:60315175..60320976hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385802
hg195802
hg185802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv942116
Samples
Known GenesADRM1, LAMA5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586485
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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