A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390601



Internal ID22448471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33063012..33075364hg38UCSC Ensembl
chr22:33458998..33471350hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3812353
hg1912353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5965493
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17390601
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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