A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458900



Internal ID236920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184972600..184987042hg38UCSC Ensembl
chr4:185893754..185908196hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3814443
hg1914443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458900
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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