A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638167



Internal ID21830214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49990627..49990724hg38UCSC Ensembl
chr22:50429056..50429153hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041513
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638167
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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