A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480808



Internal ID21138361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77766956..77776968hg38UCSC Ensembl
chr14:78233299..78243311hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3810013
hg1910013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194179
Samples
Known GenesC14orf178
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480808
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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