A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468838



Internal ID21126391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63421301..63430500hg38UCSC Ensembl
chr11:63188773..63197972hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg389200
hg199200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1208n223
Supporting Variantsnssv18177172
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468838
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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