A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760883



Internal ID20536743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37288661..37288661hg38UCSC Ensembl
chr8:37146179..37146179hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg385961
hg195961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285364
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760883
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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