A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474854



Internal ID252505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15982000..16018000hg38UCSC Ensembl
chr10:16023999..16059999hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3836001
hg1936001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474854
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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