A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930886



Internal ID22706160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84492883..84504009hg38UCSC Ensembl
chr14:84959227..84970353hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3811127
hg1911127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375802
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930886
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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