A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943786



Internal ID22719240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101426037..101426135hg38UCSC Ensembl
chr14:101892374..101892472hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378243
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943786
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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