A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290745



Internal ID20499963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85344148..85344236hg38UCSC Ensembl
chr8:86256377..86256465hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736720
Supporting Variants
Samples
Known GenesCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290745
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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