A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460463



Internal ID238444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132987329..132988979hg38UCSC Ensembl
chr5:132323021..132324671hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381651
hg191651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460463
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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