A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508899



Internal ID20882203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93417701..93421000hg38UCSC Ensembl
chr14:93884047..93887346hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022883
Samples
Known GenesUNC79
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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