A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259282



Internal ID20826322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215943754..215944262hg38UCSC Ensembl
chr2:216808477..216808985hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546171
Supporting Variants
Samples
Known GenesMREG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259282
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00056


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