A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472368



Internal ID21129921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129275801..129282000hg38UCSC Ensembl
chr11:129145696..129151895hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183508
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472368
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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