A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937146



Internal ID22712509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106011934..106627291hg38UCSC Ensembl
chr14:106478120..107083296hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38615358
hg19605177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv671n209
Supporting Variantsnssv17378095
Samples
Known GenesLINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937146
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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