A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046475



Internal ID21955719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38208577..38209795hg38UCSC Ensembl
chr22:38604584..38605802hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381219
hg191219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649262
Samples
Known GenesMAFF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046475
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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