A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5553936



Internal ID327134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25402980..25403031hg38UCSC Ensembl
chr10:25691909..25691960hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031785
Samples
Known GenesGPR158
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5553936
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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