A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465989



Internal ID21123542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115683654..115699421hg38UCSC Ensembl
chr11:115554372..115570139hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3815768
hg1915768
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177242
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465989
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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