A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478318



Internal ID21135871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55077961..55083709hg38UCSC Ensembl
chr14:55544679..55550427hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg385749
hg195749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478318
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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