A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253257



Internal ID20820297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8173262..8175087hg38UCSC Ensembl
chr1:8233322..8235147hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg381826
hg191826
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535696
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253257
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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