A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403564



Internal ID21061117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:110123801..110153100hg38UCSC Ensembl
chr5:109459502..109488801hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3829300
hg1929300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5887n223
Supporting Variantsnssv18213333
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403564
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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