A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473354



Internal ID21130907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19592416..19634113hg38UCSC Ensembl
chr12:19745350..19787047hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3841698
hg1941698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190469
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473354
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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