A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548322



Internal ID20921514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:7199801..7280500hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3880700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548322
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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