A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7625n54



Internal ID22775520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58890223..58892076hg38UCSC Ensembl
chr20:57465278..57467131hg19UCSC Ensembl
chr20:56898673..56900526hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg381854
hg191854
hg181854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586354, nsv586356, nsv586355, nsv586362, nsv586361, nsv586357, nsv586364
Samples
Known GenesGNAS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7625n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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