A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8751n54



Internal ID22776646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177576293..177579658hg38UCSC Ensembl
chr3:177294081..177297446hg19UCSC Ensembl
chr3:178776775..178780140hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg383366
hg193366
hg183366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592621, nsv592620, nsv592619
Samples
Known GenesLINC00578
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8751n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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