A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239061



Internal ID20806101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92855276..92857749hg38UCSC Ensembl
chr15:93398506..93400979hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382474
hg192474
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577089
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239061
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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