A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221296



Internal ID20788336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112844530..112845862hg38UCSC Ensembl
chr10:114604289..114605621hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381333
hg191333
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583181
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221296
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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