A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217248



Internal ID20784288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92035523..92036746hg38UCSC Ensembl
chr10:93795280..93796503hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg381224
hg191224
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591216
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217248
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00076


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