A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13700556



Internal ID21222395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176371499..176371499hg38UCSC Ensembl
chr5:175798502..175798502hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2811589
Supporting Variants
Samples
Known GenesARL10
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13700556
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.759259


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