A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224135



Internal ID20791175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63660959..63661862hg38UCSC Ensembl
chr10:65420719..65421622hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38904
hg19904
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588492
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224135
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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