A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11n100



Internal ID20151627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2777886..3350773hg38UCSC Ensembl
chr1:2694433..3267337hg19UCSC Ensembl
chr1:2684293..3257197hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38572888
hg19572905
hg18572905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010950, nsv1010228
Samples
Known GenesACTRT2, LINC00982, MIR4251, PRDM16, TTC34
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv11n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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