A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv826n54



Internal ID22768721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223916290..224029055hg38UCSC Ensembl
chr1:224103992..224216757hg19UCSC Ensembl
chr1:222170615..222283380hg18UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg38112766
hg19112766
hg18112766
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv549243, nsv549241
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv826n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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