A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6029n223



Internal ID22808997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180927301..181088900hg38UCSC Ensembl
chr5:180354301..180515900hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38161600
hg19161600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6409856, nsv6409795
Samples
Known GenesBTNL3, BTNL8, BTNL9, MIR8089
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6029n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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