A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484783



Internal ID21142336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76859326..76871911hg38UCSC Ensembl
chr14:77325669..77338254hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3812586
hg1912586
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192242
Samples
Known GenesC14orf166B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484783
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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