A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5781n223



Internal ID22808749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67709501..67717500hg38UCSC Ensembl
chr5:67005329..67013328hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6401736, nsv6409301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5781n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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