A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8974n54



Internal ID22776869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:12359578..12382323hg38UCSC Ensembl
chr4:12361202..12383947hg19UCSC Ensembl
chr4:11970300..11993045hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3822746
hg1922746
hg1822746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593746, nsv593747
SamplesHGDP00724, HGDP01035, HGDP01271, HGDP00940, HGDP00914
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8974n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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