A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748731



Internal ID20524758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27290531..27295546hg38UCSC Ensembl
chr8:27148048..27153063hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg385016
hg195016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283854
Samples
Known GenesTRIM35
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748731
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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