A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250254



Internal ID20817294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193935197..194457605hg38UCSC Ensembl
chr1:193904327..194426735hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38522409
hg19522409
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540666
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250254
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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