A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560791



Internal ID333789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170165830..170165850hg38UCSC Ensembl
chr3:169883618..169883638hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16942479
Samples
Known GenesPHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560791
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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