A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439784



Internal ID21097337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22046302..22228838hg38UCSC Ensembl
chr11:22067848..22250384hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38182537
hg19182537
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv989n223
Supporting Variantsnssv18188473
Samples
Known GenesANO5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439784
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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