A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2793792



Internal ID21239130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37652725..37652725hg38UCSC Ensembl
chr13:38226862..38226862hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13678688
Samples
Known GenesTRPC4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2793792
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