A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3389n223



Internal ID22806357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63634465..63655700hg38UCSC Ensembl
chr18:61301699..61322934hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3821236
hg1921236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6532632, nsv6521194
Samples
Known GenesSERPINB3, SERPINB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3389n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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