A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463277



Internal ID21120830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94641867..94647043hg38UCSC Ensembl
chr11:94375033..94380209hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385177
hg195177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1277n223
Supporting Variantsnssv18178545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463277
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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