A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969520



Internal ID22744455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72838906..72838906hg38UCSC Ensembl
chr14:73305614..73305614hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388490
Samples
Known GenesDPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969520
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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