A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535682



Internal ID20909036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12332001..12421700hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3889700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4624n223
Supporting Variantsnssv18204487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535682
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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