A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7779n54



Internal ID22775674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18682124..18706106hg38UCSC Ensembl
chr21:20054442..20078424hg19UCSC Ensembl
chr21:18976313..19000295hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3823983
hg1923983
hg1823983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587151, nsv587147, nsv587142
SamplesHGDP00641
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7779n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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