A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv221n54



Internal ID22768116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:30081837..30705816hg38UCSC Ensembl
chr1:30554684..31178663hg19UCSC Ensembl
chr1:30327271..30951250hg18UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38623980
hg19623980
hg18623980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545928, nsv545926, nsv545927, nsv545930
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv221n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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