A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937075



Internal ID22712438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105589326..105860333hg38UCSC Ensembl
chr14:106055663..106326543hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38271008
hg19270881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv632n209
Supporting Variantsnssv17377259
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937075
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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