A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263134



Internal ID20472352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31203675..31203675hg38UCSC Ensembl
chr4:31205297..31205297hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765292
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263134
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