A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699906



Internal ID21221739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21057597..21057597hg38UCSC Ensembl
chr10:21346526..21346526hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2788859
Supporting Variants
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699906
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.477273


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