A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480239



Internal ID21137792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20324333..20330630hg38UCSC Ensembl
chr14:20792492..20798789hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg386298
hg196298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016546
Samples
Known GenesCCNB1IP1, SNORD126
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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