A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459424



Internal ID21116977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:83942991..84009266hg38UCSC Ensembl
chr12:84336770..84403045hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3866276
hg1966276
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459424
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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