A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455913



Internal ID21113466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73834637..73842576hg38UCSC Ensembl
chr11:73545682..73553621hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg387940
hg197940
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180517
Samples
Known GenesMRPL48
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455913
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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