A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570047



Internal ID20943118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170264404..170264988hg38UCSC Ensembl
chr3:169982192..169982776hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260504
Samples
Known GenesPRKCI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570047
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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