A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484764



Internal ID21142317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42422333..42422891hg38UCSC Ensembl
chr14:42891536..42892094hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484764
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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