A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486931



Internal ID21144484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38363935..38373416hg38UCSC Ensembl
chr14:38833139..38842620hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg389482
hg199482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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