A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212978



Internal ID20780018
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 StatusS
Merged Variantsnsv6367168
Supporting Variants
Samples
Known GenesMAGI1, MAGI1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212978
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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