A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470237



Internal ID21127790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:28199901..28202100hg38UCSC Ensembl
chr12:28352834..28355033hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191954
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470237
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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