A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5418088



Internal ID197269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31980125..31981806hg38UCSC Ensembl
chr1:32445726..32447407hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381682
hg191682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16901944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5418088
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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