A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17540682



Internal ID21865037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:78914165..78914165hg38UCSC Ensembl
chr4:79835319..79835319hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6064814
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17540682
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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