A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489204



Internal ID266492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43401091..43401168hg38UCSC Ensembl
chr10:43896539..43896616hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032758
Samples
Known GenesHNRNPF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489204
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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