A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264834



Internal ID20831874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154668726..154669905hg38UCSC Ensembl
chr4:155589878..155591057hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg381180
hg191180
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561470
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264834
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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