A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9266n54



Internal ID22777161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:130994430..131442599hg38UCSC Ensembl
chr4:131915585..132363754hg19UCSC Ensembl
chr4:132135035..132583204hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38448170
hg19448170
hg18448170
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv595423, nsv595426, nsv595430, nsv595424, nsv595427, nsv595431, nsv595429
Samples1780862457_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9266n54
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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