A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420299



Internal ID199404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:4358792..4369942hg38UCSC Ensembl
chr1:4418852..4430002hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3811151
hg1911151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16906074
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420299
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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