A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504355



Internal ID20877616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89515600..89517193hg38UCSC Ensembl
chr14:89981944..89983537hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg381594
hg191594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022670
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504355
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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