A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222829



Internal ID20789869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102193956..102194484hg38UCSC Ensembl
chr10:103953713..103954241hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593509
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222829
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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