A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687446



Internal ID21209303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6210535..6210884hg38UCSC Ensembl
chr10:6252498..6252847hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789248
Supporting Variants
Samples
Known GenesPFKFB3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687446
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.52381


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