A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439492



Internal ID218028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58808000..58818000hg38UCSC Ensembl
chr3:58793726..58803726hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3810001
hg1910001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734864
Samples
Known GenesC3orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439492
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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