A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382220



Internal ID21039773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2090525..2256652hg38UCSC Ensembl
chr5:2090639..2256766hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38166128
hg19166128
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215652
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382220
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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