A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187715



Internal ID20754755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130486101..130488000hg38UCSC Ensembl
chr11:130355996..130357895hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455890
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187715
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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