A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484441



Internal ID261853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18712745..18772505hg38UCSC Ensembl
chr10:19001674..19061434hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3859761
hg1959761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484441
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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