A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474834



Internal ID21132387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:65273901..65283900hg38UCSC Ensembl
chr12:65667681..65677680hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190734
Samples
Known GenesMSRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474834
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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