A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251089



Internal ID20818129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45577855..45579504hg38UCSC Ensembl
chr1:46043527..46045176hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251089
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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