A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239025



Internal ID20806065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42845540..42846460hg38UCSC Ensembl
chr15:43137738..43138658hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38921
hg19921
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585033
Supporting Variants
Samples
Known GenesTTBK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239025
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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