A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367168



Internal ID21024721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65723733..65903057hg38UCSC Ensembl
chr3:65709408..65888732hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38179325
hg19179325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212978
Samples
Known GenesMAGI1, MAGI1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367168
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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