A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954469



Internal ID16956656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:42027509..42034308hg38UCSC Ensembl
Outerchr3:42069001..42075800hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001365
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954469
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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