A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488827



Internal ID266122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78771162..78771252hg38UCSC Ensembl
chr8:79683397..79683487hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17013869
Samples
Known GenesIL7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488827
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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