A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9552n54



Internal ID22777447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5511877..5672464hg38UCSC Ensembl
chr5:5511990..5672577hg19UCSC Ensembl
chr5:5564990..5725577hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38160588
hg19160588
hg18160588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596943, nsv596941
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9552n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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