A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991703



Internal ID61894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10219745..10219745hg38UCSC Ensembl
chr7:10259372..10259372hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536900
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991703
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001721


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