A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266447



Internal ID20833487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82434484..82435099hg38UCSC Ensembl
chr4:83355637..83356252hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565465
Supporting Variants
Samples
Known GenesENOPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266447
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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