A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9826n54



Internal ID22777721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65924514..65926514hg38UCSC Ensembl
chr5:65220342..65222342hg19UCSC Ensembl
chr5:65256098..65258098hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg382001
hg192001
hg182001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598394, nsv598393
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9826n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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