A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181296



Internal ID20748336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133741120..133866238hg38UCSC Ensembl
chr11:133611015..133736133hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38125119
hg19125119
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472328
Supporting Variants
Samples
Known GenesSPATA19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181296
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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