A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727421



Internal ID151087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12210000..12225555hg38UCSC Ensembl
chrUn_gl000235:17206..32768hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3815556
hg1915563
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419812
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727421
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.48762


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