A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253918



Internal ID20820958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84531403..84532431hg38UCSC Ensembl
chr1:84997086..84998114hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381029
hg191029
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550858
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253918
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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