A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7627n54



Internal ID22775522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58890396..58895610hg38UCSC Ensembl
chr20:57465451..57470665hg19UCSC Ensembl
chr20:56898846..56904060hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg385215
hg195215
hg185215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586360, nsv586363
Samples
Known GenesGNAS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7627n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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