A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906076



Internal ID4851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:4381732..4382056hg38UCSC Ensembl
chr1:4441792..4442116hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415439
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906076
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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