A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5792n223



Internal ID22808760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77475701..77611826hg38UCSC Ensembl
chr5:76771526..76907651hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38136126
hg19136126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6409578, nsv6396262
Samples
Known GenesWDR41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5792n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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