A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479307



Internal ID21136860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86404886..86439794hg38UCSC Ensembl
chr14:86871230..86906138hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3834909
hg1934909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479307
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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