A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273394



Internal ID20840434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27055640..27056917hg38UCSC Ensembl
chr7:27095259..27096536hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg381278
hg191278
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273394
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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