A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492172



Internal ID269392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5969655..5969746hg38UCSC Ensembl
chr10:6011618..6011709hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030563
Samples
Known GenesIL15RA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492172
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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