A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727400



Internal ID151066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11628747..11629803hg38UCSC Ensembl
chrUn_gl000229:17372..18428hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381057
hg191057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544004
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727400
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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