A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196528



Internal ID20763568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65159793..65175552hg38UCSC Ensembl
chr11:64927264..64943023hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3815760
hg1915760
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464993
Supporting Variants
Samples
Known GenesSPDYC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196528
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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