A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968328



Internal ID22743264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97204854..97204854hg38UCSC Ensembl
chr14:97671191..97671191hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375857
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968328
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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