A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4339n100



Internal ID22790426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60972596..61015133hg38UCSC Ensembl
chr20:59547652..59590189hg19UCSC Ensembl
chr20:58981047..59023584hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3842538
hg1942538
hg1842538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063006, nsv1056751
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4339n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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