A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941077



Internal ID22716495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105863143..106578855hg38UCSC Ensembl
chr14:106329353..107034840hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38715713
hg19705488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv671n209
Supporting Variantsnssv17372003
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941077
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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