A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586633



Internal ID16027356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63737667..63741460hg38UCSC Ensembl
Innerchr20:62369020..62372813hg19UCSC Ensembl
Innerchr20:61839464..61843257hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg383794
hg193794
hg183794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv943867, nssv943866
Samples
Known GenesLIME1, SLC2A4RG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586633
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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