A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060157



Internal ID21969390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29643983..29644036hg38UCSC Ensembl
chr22:30039972..30040025hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639325
Samples
Known GenesNF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060157
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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