A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249621



Internal ID20816661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:190882353..190883582hg38UCSC Ensembl
chr1:190851483..190852712hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg381230
hg191230
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553315
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249621
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00063


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