A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459445



Internal ID21116998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:84519652..84587628hg38UCSC Ensembl
chr12:84913431..84981407hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3867977
hg1967977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183804
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459445
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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