A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462437



Internal ID240365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92487349..92487600hg38UCSC Ensembl
chr4:93408500..93408751hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16952710
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462437
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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