A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241040



Internal ID20808080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55321678..55322193hg38UCSC Ensembl
chr15:55613876..55614391hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38516
hg19516
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583978
Supporting Variants
Samples
Known GenesPIGB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241040
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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