A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182213



Internal ID20749253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90732696..90743429hg38UCSC Ensembl
chr11:90465864..90476597hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3810734
hg1910734
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464477
Supporting Variants
Samples
Known GenesDISC1FP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182213
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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