A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563322



Internal ID20936393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179173729..179174327hg38UCSC Ensembl
chr3:178891517..178892115hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38599
hg19599
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263354
Samples
Known GenesPIK3CA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563322
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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