A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587668



Internal ID21536226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75317928..75319281hg38UCSC Ensembl
chr14:75784631..75785984hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381354
hg191354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080496
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587668
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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