A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188956



Internal ID20755996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90139338..90291765hg38UCSC Ensembl
chr11:89872506..90024933hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38152428
hg19152428
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475215
Supporting Variants
Samples
Known GenesCHORDC1, DISC1FP1, NAALAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188956
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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