A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932525



Internal ID22707825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89876235..89877092hg38UCSC Ensembl
chr14:90342579..90343436hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38858
hg19858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373030
Samples
Known GenesEFCAB11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932525
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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