A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269255



Internal ID20836295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14930962..14931570hg38UCSC Ensembl
chr6:14931193..14931801hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569574
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269255
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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