A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4342n100



Internal ID22790429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61439901..61515326hg38UCSC Ensembl
chr20:60014957..60090382hg19UCSC Ensembl
chr20:59448352..59523777hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3875426
hg1975426
hg1875426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1067387, nsv1060501, nsv1065583, nsv1058517
Samples
Known GenesCDH4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4342n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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