A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590608



Internal ID21539177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90525388..90525993hg38UCSC Ensembl
chr14:90991732..90992337hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098256
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590608
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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