A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474123



Internal ID21131676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69662555..69666405hg38UCSC Ensembl
chr12:70056335..70060185hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg383851
hg193851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002510
Samples
Known GenesBEST3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474123
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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