A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465092



Internal ID242962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72660371..72745965hg38UCSC Ensembl
chr5:71956198..72041792hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3885595
hg1985595
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16967521
Samples
Known GenesLOC102477328
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465092
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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