A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048095



Internal ID21957328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27049134..27057586hg38UCSC Ensembl
chr22:27445096..27453548hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg388453
hg198453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641692
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048095
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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