A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240227



Internal ID20807267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44344251..44344596hg38UCSC Ensembl
chr15:44636449..44636794hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594941
Supporting Variants
Samples
Known GenesCASC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240227
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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