A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5633n223



Internal ID22808601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8699301..8733600hg38UCSC Ensembl
chr5:8699413..8733712hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3834300
hg1934300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6388118, nsv6387006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5633n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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