A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625509



Internal ID21817556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15581224..15581224hg38UCSC Ensembl
chr19:15692035..15692035hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109816
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625509
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