A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266843



Internal ID20833883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139086387..139086893hg38UCSC Ensembl
chr5:138422076..138422582hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38507
hg19507
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570773
Supporting Variants
Samples
Known GenesSIL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266843
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00029


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