A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238096



Internal ID20805137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50385293..50386027hg38UCSC Ensembl
chr15:50677490..50678224hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580638
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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