A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459065



Internal ID237084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34969472..34976965hg38UCSC Ensembl
chr5:34969577..34977070hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg387494
hg197494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16964238
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459065
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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