A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507500



Internal ID284217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59957001..60041131hg38UCSC Ensembl
chr14:60423719..60507849hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3884131
hg1984131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698032
Samples
Known GenesLRRC9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507500
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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