A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228809



Internal ID20795849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13134064..13136181hg38UCSC Ensembl
chr10:13176064..13178181hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382118
hg192118
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592442
Supporting Variants
Samples
Known GenesOPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228809
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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