A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457218



Internal ID21114771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95652121..95713598hg38UCSC Ensembl
chr11:95385285..95446762hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3861478
hg1961478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194554
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457218
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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