A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473441



Internal ID21130994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116069255..116074387hg38UCSC Ensembl
chr11:115939973..115945105hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385133
hg195133
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473441
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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