A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272821



Internal ID20839861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99290487..99290841hg38UCSC Ensembl
chr6:99738363..99738717hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565522
Supporting Variants
Samples
Known GenesFAXC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272821
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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