A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452372



Internal ID230527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59036775..59066841hg38UCSC Ensembl
chr3:59022501..59052567hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3830067
hg1930067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934595
Samples
Known GenesC3orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452372
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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