A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931309



Internal ID22706591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105863258..106639118hg38UCSC Ensembl
chr14:106329468..107095123hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38775861
hg19765656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv671n209
Supporting Variantsnssv17381886
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931309
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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