A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486295



Internal ID21143848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42206694..42501534hg38UCSC Ensembl
chr14:42675897..42970737hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38294841
hg19294841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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