A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9956n54



Internal ID22777851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99008867..99021711hg38UCSC Ensembl
chr5:98344571..98357415hg19UCSC Ensembl
chr5:98372471..98385315hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3812845
hg1912845
hg1812845
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv599093, nsv599107, nsv599103, nsv599113
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9956n54
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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