A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241111



Internal ID20808151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56712416..56712741hg38UCSC Ensembl
chr15:57004614..57004939hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584723
Supporting Variants
Samples
Known GenesZNF280D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241111
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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