A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436857



Internal ID215465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158311085..158331736hg38UCSC Ensembl
chr3:158028874..158049525hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3820652
hg1920652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941950
Samples
Known GenesRSRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436857
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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