A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462886



Internal ID240808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84538489..84542314hg38UCSC Ensembl
chr4:85459642..85463467hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg383826
hg193826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16953607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462886
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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