A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251909



Internal ID20818949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86878565..86880381hg38UCSC Ensembl
chr1:87344248..87346064hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381817
hg191817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543467
Supporting Variants
Samples
Known GenesSEP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251909
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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