A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181212



Internal ID20748252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99025658..99067378hg38UCSC Ensembl
chr13:99677912..99719632hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3841721
hg1941721
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489915
Supporting Variants
Samples
Known GenesDOCK9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181212
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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