A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483441



Internal ID21140994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83971248..84192353hg38UCSC Ensembl
chr14:84437592..84658697hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg38221106
hg19221106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022272
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483441
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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