A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903642



Internal ID3244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32639057..32643777hg38UCSC Ensembl
chr1:33104658..33109378hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg384721
hg194721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416363
Supporting Variants
Samples
Known GenesZBTB8OS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903642
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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