A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7626n54



Internal ID22775521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58890396..58893423hg38UCSC Ensembl
chr20:57465451..57468478hg19UCSC Ensembl
chr20:56898846..56901873hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg383028
hg193028
hg183028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586359, nsv586366, nsv586365
Samples
Known GenesGNAS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7626n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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