A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270989



Internal ID20480207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25898780..25898780hg38UCSC Ensembl
chr15:26143927..26143927hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757973
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270989
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