A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2793057



Internal ID21238395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112215112..112215112hg38UCSC Ensembl
chr13:112869426..112869426hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13691917
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2793057
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