A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250653



Internal ID20817693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233291488..233292405hg38UCSC Ensembl
chr1:233427234..233428151hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539031
Supporting Variants
Samples
Known GenesPCNXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250653
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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