A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484917



Internal ID262316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16242983..16250064hg38UCSC Ensembl
chr10:16284982..16292063hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg387082
hg197082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030376
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484917
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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