A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186238



Internal ID20753279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96615843..96636927hg38UCSC Ensembl
chr13:97268097..97289181hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3821085
hg1921085
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482980
Supporting Variants
Samples
Known GenesHS6ST3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186238
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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