A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424453



Internal ID203444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9439594..9443739hg38UCSC Ensembl
chr1:9499653..9503798hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg384146
hg194146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424453
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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