A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484467



Internal ID21142020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:40686274..40750311hg38UCSC Ensembl
chr14:41155479..41219516hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3864038
hg1964038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484467
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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