A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480820



Internal ID21138373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64884039..64901316hg38UCSC Ensembl
chr14:65350757..65368034hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3817278
hg1917278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020710
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480820
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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