A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5538763



Internal ID313811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100026381..100026381hg38UCSC Ensembl
chr14:100492718..100492718hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5538763
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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