A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746886



Internal ID20522902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11782782..11782908hg38UCSC Ensembl
chr8:11640291..11640417hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265538
Samples
Known GenesNEIL2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746886
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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