A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932106



Internal ID22707399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70611881..70612014hg38UCSC Ensembl
chr14:71078598..71078731hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384997
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932106
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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