A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238934



Internal ID20805974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66326992..66327445hg38UCSC Ensembl
chr15:66619330..66619783hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38454
hg19454
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584155
Supporting Variants
Samples
Known GenesDIS3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238934
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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