A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265538



Internal ID20474756
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 StatusS
Merged Variantsnsv4746886
Supporting Variants
Samples
Known GenesNEIL2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265538
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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