A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955319



Internal ID17304192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:14982594..14991593hg38UCSC Ensembl
Outerchr3:15024101..15033100hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001339
SamplesBILGI_BIOE
Known GenesNR2C2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955319
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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