A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259555



Internal ID20826595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:125581239..125581643hg38UCSC Ensembl
chr3:125300083..125300487hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559342
Supporting Variants
Samples
Known GenesOSBPL11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259555
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00019


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