A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483408



Internal ID21140961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27354380..27422109hg38UCSC Ensembl
chr14:27823586..27891315hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3867730
hg1967730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2082n223
Supporting Variantsnssv18016672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483408
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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