A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273359



Internal ID20840399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26226588..26227217hg38UCSC Ensembl
chr7:26266208..26266837hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559795
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273359
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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