A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238877



Internal ID20805917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65170883..65171342hg38UCSC Ensembl
chr15:65463221..65463680hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590292
Supporting Variants
Samples
Known GenesCLPX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238877
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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