A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264673



Internal ID20831713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75663399..75663710hg38UCSC Ensembl
chr4:76588583..76588894hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567360
Supporting Variants
Samples
Known GenesG3BP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264673
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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