A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523035



Internal ID21847394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238938132..238938132hg38UCSC Ensembl
chr1:239101432..239101432hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056301
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523035
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