A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250689



Internal ID20817729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235228071..235230278hg38UCSC Ensembl
chr1:235391386..235393593hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg382208
hg192208
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535708
Supporting Variants
Samples
Known GenesARID4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250689
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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