A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479441



Internal ID21136994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:80755456..80756047hg38UCSC Ensembl
chr14:81221800..81222391hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021347
Samples
Known GenesCEP128
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479441
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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