A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465418



Internal ID21122971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:65975673..65983035hg38UCSC Ensembl
chr12:66369453..66376815hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg387363
hg197363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465418
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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