A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263425



Internal ID20830465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:104924030..104930941hg38UCSC Ensembl
chr4:105845187..105852098hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg386912
hg196912
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557879
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263425
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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