A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464402



Internal ID21121955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70452238..70452331hg38UCSC Ensembl
chr11:70298343..70298436hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464402
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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