A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9148n54



Internal ID20142572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86056551..86058430hg38UCSC Ensembl
chr4:86977704..86979583hg19UCSC Ensembl
chr4:87196728..87198607hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg381880
hg191880
hg181880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594774, nsv594778, nsv594775, nsv594777
Samples
Known GenesMAPK10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9148n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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