A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219831



Internal ID20786871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130147835..130148377hg38UCSC Ensembl
chr10:131946099..131946641hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582416
Supporting Variants
Samples
Known GenesGLRX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219831
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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