A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249852



Internal ID20816892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:115916230..115917100hg38UCSC Ensembl
chr1:116458851..116459721hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536361
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249852
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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