A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288323



Internal ID20497541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26002841..26002904hg38UCSC Ensembl
chr8:25860357..25860420hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735314
Supporting Variants
Samples
Known GenesEBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288323
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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