A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241847



Internal ID20808887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59979898..59980411hg38UCSC Ensembl
chr15:60272097..60272610hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591138
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241847
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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