A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268838



Internal ID20835878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3679800..4779377hg38UCSC Ensembl
chr5:3679914..4779490hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg381099578
hg191099577
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571563
Supporting Variants
Samples
Known GenesLOC101929153
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268838
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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