A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954886



Internal ID16957073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:72374650..72446149hg38UCSC Ensembl
Outerchr3:72423801..72495300hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3871500
hg1971500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001413
SamplesBILGI_BIOE
Known GenesRYBP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954886
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