A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538481



Internal ID20911798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42254275..42260711hg38UCSC Ensembl
chr22:42650281..42656717hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg386437
hg196437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074561
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538481
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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