A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266083



Internal ID20833123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85344162..85369202hg38UCSC Ensembl
chr4:86265315..86290355hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3825041
hg1925041
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556632
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266083
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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