A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4290n100



Internal ID20155906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25086650..25494993hg38UCSC Ensembl
chr20:25067286..25475629hg19UCSC Ensembl
chr20:25015286..25423629hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38408344
hg19408344
hg18408344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063016, nsv1062742, nsv1063494
Samples
Known GenesABHD12, ENTPD6, GINS1, LOC284798, NINL, PYGB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4290n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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