A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13709780



Internal ID21231556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67538278..67538607hg38UCSC Ensembl
chr9:65906803..65907106hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38330
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819700
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13709780
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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