A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508114



Internal ID20881412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104918223..105014225hg38UCSC Ensembl
chr14:105384560..105480562hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3896003
hg1996003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197105
Samples
Known GenesAHNAK2, C14orf79, CDCA4, PLD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508114
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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