A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238080



Internal ID20805120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50218206..50218403hg38UCSC Ensembl
chr15:50510403..50510600hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592507
Supporting Variants
Samples
Known GenesSLC27A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238080
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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