A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231179



Internal ID20798219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43135463..43136052hg38UCSC Ensembl
chr10:43630911..43631500hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580193
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231179
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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