A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486832



Internal ID21144385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36674730..36675943hg38UCSC Ensembl
chr14:37143935..37145148hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg381214
hg191214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017973
Samples
Known GenesPAX9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486832
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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