A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264372



Internal ID20831412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169209345..169209821hg38UCSC Ensembl
chr4:170130496..170130972hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564019
Supporting Variants
Samples
Known GenesSH3RF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264372
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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