A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4346n100



Internal ID22790433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64086577..64131053hg38UCSC Ensembl
chr20:62717930..62762406hg19UCSC Ensembl
chr20:62188374..62232850hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3844477
hg1944477
hg1844477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060601, nsv1057039
Samples
Known GenesNPBWR2, OPRL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4346n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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