A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483569



Internal ID21141122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:53324201..53341300hg38UCSC Ensembl
chr14:53790919..53808018hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3817100
hg1917100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020052
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483569
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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