A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483988



Internal ID21141541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60060738..60095333hg38UCSC Ensembl
chr14:60527456..60562051hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3834596
hg1934596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020473
Samples
Known GenesLRRC9, PCNXL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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