A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218466



Internal ID20785506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36969695..36970395hg38UCSC Ensembl
chr13:37543832..37544532hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595180
Supporting Variants
Samples
Known GenesALG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218466
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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