A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293734



Internal ID20502952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73067663..73067663hg38UCSC Ensembl
chr8:73979898..73979898hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763349
Supporting Variants
Samples
Known GenesSBSPON
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293734
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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