A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269187



Internal ID20836227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65542470..65542772hg38UCSC Ensembl
chr5:64838297..64838599hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574405
Supporting Variants
Samples
Known GenesCENPK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269187
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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