A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2805116



Internal ID21250454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11112784..11112784hg38UCSC Ensembl
chr2:11252910..11252910hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13695992
Samples
Known GenesFLJ33534
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2805116
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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