A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272467



Internal ID20839507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138694764..138696112hg38UCSC Ensembl
chr6:139015901..139017249hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg381349
hg191349
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556867
Supporting Variants
Samples
Known GenesFLJ46906
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272467
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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