A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763349



Internal ID20539209
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 StatusM
Merged Variants
Supporting Variantsnssv16293734
Samples
Known GenesSBSPON
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763349
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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