A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943300



Internal ID22718747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105864354..106810391hg38UCSC Ensembl
chr14:106330564..107218625hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38946038
hg19888062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv647n209
Supporting Variantsnssv17372292
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943300
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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