A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9312n54



Internal ID20142736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150944370..151059484hg38UCSC Ensembl
chr4:151865522..151980636hg19UCSC Ensembl
chr4:152084972..152200086hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38115115
hg19115115
hg18115115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv595699, nsv595692
SamplesHGDP00241
Known GenesLRBA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9312n54
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