A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv446n54



Internal ID22768341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:104347464..104411743hg38UCSC Ensembl
chr1:104890086..104954365hg19UCSC Ensembl
chr1:104691609..104755888hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3864280
hg1964280
hg1864280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv547212, nsv547214, nsv547213
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv446n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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