A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270677



Internal ID20837717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35650314..35650769hg38UCSC Ensembl
chr6:35618091..35618546hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559075
Supporting Variants
Samples
Known GenesFKBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270677
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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