A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221905



Internal ID20788945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58392969..58393888hg38UCSC Ensembl
chr10:60152729..60153648hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38920
hg19920
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585869
Supporting Variants
Samples
Known GenesTFAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221905
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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