A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489057



Internal ID21146610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35027629..35047708hg38UCSC Ensembl
chr14:35496835..35516914hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3820080
hg1920080
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187799
Samples
Known GenesFAM177A1, SRP54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489057
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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