A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455295



Internal ID21112848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30731392..30770603hg38UCSC Ensembl
chr11:30752939..30792150hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3839212
hg1939212
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178136
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455295
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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