A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190268



Internal ID20757308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120564547..120577028hg38UCSC Ensembl
chr11:120435256..120447737hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3812482
hg1912482
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471919
Supporting Variants
Samples
Known GenesGRIK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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