A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466547



Internal ID244380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155602008..155604423hg38UCSC Ensembl
chr4:156523160..156525575hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382416
hg192416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16957249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466547
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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