A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685608



Internal ID21207468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45890319..45890319hg38UCSC Ensembl
chr3:45931811..45931811hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807537
Supporting Variants
Samples
Known GenesCCR9, LZTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685608
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.984375


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