A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16896349



Internal ID171718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223989621..223992673hg38UCSC Ensembl
chr1:224177323..224180375hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg383053
hg193053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453302
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16896349
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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