A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262485



Internal ID20829525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142708261..142709721hg38UCSC Ensembl
chr3:142427103..142428563hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381461
hg191461
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560344
Supporting Variants
Samples
Known GenesPLS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262485
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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