A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466297



Internal ID21123850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:18727167..18732216hg38UCSC Ensembl
chr12:18880101..18885150hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg385050
hg195050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999602
Samples
Known GenesPLCZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466297
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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