A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489382



Internal ID21146935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23926212..23928034hg38UCSC Ensembl
chr14:24395421..24397243hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381823
hg191823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016764
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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