A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489510



Internal ID21147063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42093008..42389606hg38UCSC Ensembl
chr14:42562211..42858809hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38296599
hg19296599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180729
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489510
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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