A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361796



Internal ID21019349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65349801..65394000hg38UCSC Ensembl
chr3:65335476..65379675hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3844200
hg1944200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212967
Samples
Known GenesMAGI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361796
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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