A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461041



Internal ID21118594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83172616..83174106hg38UCSC Ensembl
chr11:82883658..82885148hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381491
hg191491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188299
Samples
Known GenesPCF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461041
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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