A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456447



Internal ID234514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1620843..1623688hg38UCSC Ensembl
chr5:1620958..1623803hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382846
hg192846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16960811
Samples
Known GenesLOC728613
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456447
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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