A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8495n54



Internal ID22776390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105719476..105751290hg38UCSC Ensembl
chr3:105438320..105470134hg19UCSC Ensembl
chr3:106921010..106952824hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3831815
hg1931815
hg1831815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591245, nsv591243
Samples
Known GenesCBLB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8495n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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