A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478689



Internal ID256237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22884709..22890214hg38UCSC Ensembl
chr10:23173638..23179143hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg385506
hg195506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv44n206
Supporting Variantsnssv17032183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478689
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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