A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476114



Internal ID21133667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25966463..25967273hg38UCSC Ensembl
chr14:26435669..26436479hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38811
hg19811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016838
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476114
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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