A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648456



Internal ID21840503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31963371..31964070hg38UCSC Ensembl
chr22:32359358..32360057hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648456
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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