A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260813



Internal ID20827853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52589937..52590434hg38UCSC Ensembl
chr3:52623953..52624450hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537241
Supporting Variants
Samples
Known GenesPBRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260813
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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