A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4325n100



Internal ID22790412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53779021..53811681hg38UCSC Ensembl
chr20:52395560..52428220hg19UCSC Ensembl
chr20:51828967..51861627hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3832661
hg1932661
hg1832661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063442, nsv1064299
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)dgv4325n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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