A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472333



Internal ID21129886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:75871213..75888513hg38UCSC Ensembl
chr12:76264993..76282293hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3817301
hg1917301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193453
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472333
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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