A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464063



Internal ID241949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6380938..6383874hg38UCSC Ensembl
chr5:6381051..6383987hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg382937
hg192937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464063
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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