A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466547



Internal ID21124100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64881327..64890240hg38UCSC Ensembl
chr11:64648799..64657712hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg388914
hg198914
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187406
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466547
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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