A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9150n54



Internal ID20142574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86057367..86058774hg38UCSC Ensembl
chr4:86978520..86979927hg19UCSC Ensembl
chr4:87197544..87198951hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg381408
hg191408
hg181408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594782, nsv594781, nsv594780
Samples
Known GenesMAPK10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9150n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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