A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250819



Internal ID20817859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32135876..32138394hg38UCSC Ensembl
chr1:32601477..32603995hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382519
hg192519
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546921
Supporting Variants
Samples
Known GenesKPNA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250819
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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