A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263681



Internal ID20830721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:124453132..124453639hg38UCSC Ensembl
chr4:125374287..125374794hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558896
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263681
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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