A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16905954



Internal ID4767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91041068..91046868hg38UCSC Ensembl
chr1:91506625..91512425hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg385801
hg195801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422609
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16905954
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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