A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727357



Internal ID151024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10840000..10870643hg38UCSC Ensembl
chrUn_gl000244:5357..36000hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3830644
hg1930644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146943
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727357
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.038496


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