A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794004



Internal ID21239342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78659304..78659304hg38UCSC Ensembl
chr13:79233439..79233439hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13683164, nssv13686029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794004
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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