A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468590



Internal ID21126143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19550628..19554634hg38UCSC Ensembl
chr12:19703562..19707568hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg384007
hg194007
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185768
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468590
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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