A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252012



Internal ID20819052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91114787..91116484hg38UCSC Ensembl
chr1:91580344..91582041hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg381698
hg191698
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550206
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252012
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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