A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486945



Internal ID264295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3913048..3913172hg38UCSC Ensembl
chr10:3955240..3955364hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029450
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486945
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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