A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224160



Internal ID20791200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124945967..124946339hg38UCSC Ensembl
chr10:126634536..126634908hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586236
Supporting Variants
Samples
Known GenesZRANB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224160
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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