A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904164



Internal ID3593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62694181..62694264hg38UCSC Ensembl
chr1:63159852..63159935hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433610
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904164
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.007649


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