A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461370



Internal ID21118923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3544075..3603994hg38UCSC Ensembl
chr12:3653241..3713160hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3859920
hg1959920
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181928
Samples
Known GenesPRMT8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461370
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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