A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481465



Internal ID21139018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22828549..22833209hg38UCSC Ensembl
chr14:23297758..23302418hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg384661
hg194661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016703
Samples
Known GenesMRPL52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481465
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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