A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5999n223



Internal ID22808967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156658801..156666900hg38UCSC Ensembl
chr5:156085812..156093911hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg388100
hg198100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6405597, nsv6411001
Samples
Known GenesSGCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5999n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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