A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230659



Internal ID20797699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21106934..21111103hg38UCSC Ensembl
chr10:21395863..21400032hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg384170
hg194170
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587060
Supporting Variants
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230659
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00013


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