A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763682



Internal ID20539542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59355435..59355435hg38UCSC Ensembl
chr20:57930490..57930490hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262322
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763682
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer