A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464809



Internal ID242680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51950931..51987855hg38UCSC Ensembl
chr4:52817097..52854021hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3836925
hg1936925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16950031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464809
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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