A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8628n54



Internal ID22776523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:144103155..144339553hg38UCSC Ensembl
chr3:143821997..144058395hg19UCSC Ensembl
chr3:145304687..145541085hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38236399
hg19236399
hg18236399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591926, nsv591925
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8628n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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