A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9881n54



Internal ID22777776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75053016..75053542hg38UCSC Ensembl
chr5:74348841..74349367hg19UCSC Ensembl
chr5:74384597..74385123hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38527
hg19527
hg18527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598670, nsv598666
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9881n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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