A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598805



Internal ID21547434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75924044..75926169hg38UCSC Ensembl
chr14:76390387..76392512hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382126
hg192126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083160
SamplesHG02011
Known GenesTTLL5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598805
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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