A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266055



Internal ID20833095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83603632..83604064hg38UCSC Ensembl
chr4:84524785..84525217hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559205
Supporting Variants
Samples
Known GenesAGPAT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266055
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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