A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485674



Internal ID21143227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25766597..25767235hg38UCSC Ensembl
chr14:26235803..26236441hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016805
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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