A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696492



Internal ID21218345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29641687..29647707hg38UCSC Ensembl
chr13:30215824..30221844hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg386021
hg196021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2792672
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696492
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.5625


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