A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942492



Internal ID22717930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97221511..97221564hg38UCSC Ensembl
chr14:97687848..97687901hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942492
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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