A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464508



Internal ID242386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75674566..75676490hg38UCSC Ensembl
chr4:76599750..76601674hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg381925
hg191925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16952989
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464508
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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