A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9955n54



Internal ID22777850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99008867..99011352hg38UCSC Ensembl
chr5:98344571..98347056hg19UCSC Ensembl
chr5:98372471..98374956hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg382486
hg192486
hg182486
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv599092, nsv599091
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9955n54
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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