A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13711019



Internal ID21232780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75172473..75172473hg38UCSC Ensembl
chr9:77787389..77787389hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819973
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13711019
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03125


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