A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535757



Internal ID20909110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35883101..35903500hg38UCSC Ensembl
chr21:37255399..37275798hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3820400
hg1920400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4595n223
Supporting Variantsnssv18203935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535757
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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