A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239716



Internal ID20806756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78056508..78056662hg38UCSC Ensembl
chr15:78348850..78349004hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590882
Supporting Variants
Samples
Known GenesTBC1D2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239716
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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