A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490951



Internal ID268199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28641550..28651184hg38UCSC Ensembl
chr10:28930479..28940113hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg389635
hg199635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033427
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490951
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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