A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291777



Internal ID20500995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100098832..100098894hg38UCSC Ensembl
chr8:101111060..101111122hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731376
Supporting Variants
Samples
Known GenesRGS22
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291777
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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