A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251926



Internal ID20818966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87639563..87640056hg38UCSC Ensembl
chr1:88105246..88105739hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545374
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251926
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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