A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224173



Internal ID20791213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111315102..111316018hg38UCSC Ensembl
chr10:113074860..113075776hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590967
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224173
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00032


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