A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416363



Internal ID195591
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 StatusM
Merged Variants
Supporting Variantsnssv16903642
Samples
Known GenesZBTB8OS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416363
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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