A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189717



Internal ID20756757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90272513..90598556hg38UCSC Ensembl
chr11:90005681..90331724hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38326044
hg19326044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462782
Supporting Variants
Samples
Known GenesDISC1FP1, MIR4490
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189717
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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