A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178029



Internal ID20745069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42999401..43006000hg38UCSC Ensembl
chr11:43020951..43027550hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464455
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178029
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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