A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586123



Internal ID16026846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45722456..45746108hg38UCSC Ensembl
Innerchr20:44351095..44374747hg19UCSC Ensembl
Innerchr20:43784509..43808154hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3823653
hg1923653
hg1823646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7592n54
Supporting Variantsnssv940854
Samples
Known GenesSPINT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586123
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