A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250290



Internal ID20817330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226774125..226774738hg38UCSC Ensembl
chr1:226961826..226962439hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538588
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250290
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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