A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563802



Internal ID336730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113225866..113225901hg38UCSC Ensembl
chr9:115988146..115988181hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg386015
hg196015
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026370
Samples
Known GenesSLC31A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563802
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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