A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520516



Internal ID21844875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8912238..8912238hg38UCSC Ensembl
chr1:8972297..8972297hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056187
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520516
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