A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683471



Internal ID21205333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29460148..29460148hg38UCSC Ensembl
chr11:29481695..29481695hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790218
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683471
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.328125


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