A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459932



Internal ID237936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18604517..18672309hg38UCSC Ensembl
chr5:18604626..18672418hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3867793
hg1967793
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16963001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459932
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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