A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275794



Internal ID20842834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98033050..98033526hg38UCSC Ensembl
chr7:97662362..97662838hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569349
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275794
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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