A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904555



Internal ID3859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67529891..67531185hg38UCSC Ensembl
chr1:67995574..67996868hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381295
hg191295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427982
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904555
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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