A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473665



Internal ID21131218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56554197..56591852hg38UCSC Ensembl
chr11:56321673..56359328hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3837656
hg1937656
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181445
Samples
Known GenesOR5M10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473665
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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