A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17649262



Internal ID21841309
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 StatusS
Merged Variantsnsv6046475
Supporting Variants
Samples
Known GenesMAFF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17649262
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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