A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv659n54



Internal ID20134083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182391461..182392329hg38UCSC Ensembl
chr1:182360596..182361464hg19UCSC Ensembl
chr1:180627219..180628087hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38869
hg19869
hg18869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv548364, nsv548365
Samples
Known GenesGLUL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv659n54
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