A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571351



Internal ID20944422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130745783..130747412hg38UCSC Ensembl
chr3:130464627..130466256hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381630
hg191630
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259645
Samples
Known GenesPIK3R4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571351
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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