A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270597



Internal ID20837637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17575772..17576136hg38UCSC Ensembl
chr6:17576003..17576367hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570765
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270597
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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