A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969984



Internal ID22744919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35976491..35976491hg38UCSC Ensembl
chr14:36445697..36445697hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969984
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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