A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479291



Internal ID256819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20837099..20843493hg38UCSC Ensembl
chr10:21126028..21132422hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg386395
hg196395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031742
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479291
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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