A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16905052



Internal ID4183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:73492157..73492265hg38UCSC Ensembl
chr1:73957840..73957948hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427867
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16905052
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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