A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7860n54



Internal ID19000036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42278986..42289572hg38UCSC Ensembl
chr21:43699096..43709682hg19UCSC Ensembl
chr21:42572165..42582751hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3810587
hg1910587
hg1810587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587629, nsv587628
Samples
Known GenesABCG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7860n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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