A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477485



Internal ID21135038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65689101..65724700hg38UCSC Ensembl
chr14:66155819..66191418hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3835600
hg1935600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2177n223
Supporting Variantsnssv18188643
Samples
Known GenesFUT8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477485
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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