A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638933



Internal ID21830980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33735842..33858438hg38UCSC Ensembl
chr22:34131828..34254426hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38122597
hg19122599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042341
Supporting Variants
Samples
Known GenesLARGE, LARGE-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638933
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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