A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4322n100



Internal ID20155938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47663210..48489530hg38UCSC Ensembl
chr20:46291954..47117776hg19UCSC Ensembl
chr20:45725361..46551183hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38826321
hg19825823
hg18825823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057888, nsv1062327
Samples
Known GenesLINC00494, SULF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4322n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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