A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259886



Internal ID20826926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173002521..173009172hg38UCSC Ensembl
chr3:172720311..172726962hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg386652
hg196652
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570875
Supporting Variants
Samples
Known GenesSPATA16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259886
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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