A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571374



Internal ID20944445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170242024..170242774hg38UCSC Ensembl
chr3:169959812..169960562hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38751
hg19751
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260502
Samples
Known GenesPRKCI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571374
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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