A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439187



Internal ID217729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75443163..75861638hg38UCSC Ensembl
chr3:75492314..75910789hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38418476
hg19418476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935801
Samples
Known GenesFLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439187
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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