A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5965n54



Internal ID22773860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62039493..62040252hg38UCSC Ensembl
chr18:59706726..59707485hg19UCSC Ensembl
chr18:57857706..57858465hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38760
hg19760
hg18760
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577081, nsv577082
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5965n54
Frequency
Sample Size17421
Observed Gain18
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer