A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483882



Internal ID261309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11711966..11713302hg38UCSC Ensembl
chr10:11753965..11755301hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381337
hg191337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483882
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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