A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4336n100



Internal ID22790423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59857564..59943263hg38UCSC Ensembl
chr20:58432619..58518318hg19UCSC Ensembl
chr20:57866014..57951713hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3885700
hg1985700
hg1885700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062955, nsv1063034, nsv1057557, nsv1058935, nsv1059559, nsv1065680
Samples
Known GenesFAM217B, PPP1R3D, SYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4336n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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