A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929899



Internal ID22705158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105589831..105860284hg38UCSC Ensembl
chr14:106056168..106326494hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38270454
hg19270327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv632n209
Supporting Variantsnssv17383946
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929899
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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