A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472887



Internal ID21130440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120328537..120329099hg38UCSC Ensembl
chr11:120199246..120199808hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188888
Samples
Known GenesTMEM136
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472887
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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