A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472413



Internal ID21129966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57016145..57033466hg38UCSC Ensembl
chr11:56783620..56800941hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3817322
hg1917322
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472413
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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