A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458464



Internal ID21116017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102342801..102353700hg38UCSC Ensembl
chr11:102213532..102224431hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3810900
hg1910900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177950
Samples
Known GenesBIRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458464
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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