A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225892



Internal ID20792932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92515751..92515976hg38UCSC Ensembl
chr10:94275508..94275733hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581212
Supporting Variants
Samples
Known GenesIDE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225892
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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