A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248903



Internal ID20815943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202336302..202338878hg38UCSC Ensembl
chr1:202305430..202308006hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382577
hg192577
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543596
Supporting Variants
Samples
Known GenesUBE2T
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248903
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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