A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586361



Internal ID16373770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58890516..58891870hg38UCSC Ensembl
Innerchr20:57465571..57466925hg19UCSC Ensembl
Innerchr20:56898966..56900320hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg381355
hg191355
hg181355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7625n54
Supporting Variantsnssv941803
Samples
Known GenesGNAS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586361
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