A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266533



Internal ID20833573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6579543..6584784hg38UCSC Ensembl
chr4:6581270..6586511hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg385242
hg195242
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562583
Supporting Variants
Samples
Known GenesMAN2B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266533
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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