A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461024



Internal ID21118577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66432173..66437656hg38UCSC Ensembl
chr11:66199644..66205127hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg385484
hg195484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992569
Samples
Known GenesMRPL11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461024
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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