A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466394



Internal ID21123947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1989901..1991100hg38UCSC Ensembl
chr12:2099067..2100266hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999670
Samples
Known GenesDCP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466394
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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