A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8563n54



Internal ID19000739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127543914..127685471hg38UCSC Ensembl
chr3:127262757..127404314hg19UCSC Ensembl
chr3:128745447..128887004hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38141558
hg19141558
hg18141558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591581, nsv591580
Samples
Known GenesABTB1, MCM2, MIR6825, PODXL2, TPRA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8563n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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