A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265660



Internal ID20832700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42166139..42168543hg38UCSC Ensembl
chr4:42168156..42170560hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg382405
hg192405
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574126
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265660
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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