A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456822



Internal ID21114375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62363678..62383200hg38UCSC Ensembl
chr11:62131150..62150672hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3819523
hg1919523
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1205n223
Supporting Variantsnssv18196277
Samples
Known GenesASRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456822
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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