A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473134



Internal ID21130687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47142242..47151400hg38UCSC Ensembl
chr11:47163793..47172951hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg389159
hg199159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189400
Samples
Known GenesC11orf49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473134
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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