A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246874



Internal ID20813915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46057375..46057908hg38UCSC Ensembl
chr18:43637341..43637874hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586755
Supporting Variants
Samples
Known GenesPSTPIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246874
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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