A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263103



Internal ID20830143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:134171656..134177442hg38UCSC Ensembl
chr4:135092811..135098597hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg385787
hg195787
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569600
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263103
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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