A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1330n209



Internal ID22827405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61714172..61741755hg38UCSC Ensembl
chr20:60289228..60316811hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3827584
hg1927584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5955662, nsv5964325
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1330n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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