A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540496



Internal ID20913789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42349024..42355607hg38UCSC Ensembl
chr22:42745030..42751613hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg386584
hg196584
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540496
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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