A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222939



Internal ID20789979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104224241..104224484hg38UCSC Ensembl
chr10:105983999..105984242hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583540
Supporting Variants
Samples
Known GenesWDR96
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222939
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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