A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117865



Internal ID21301131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32439762..32911564hg38UCSC Ensembl
Innerchr10:32728690..33200492hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38471803
hg19471803
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088753
Samplessample302
Known GenesCCDC7, ITGB1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117865
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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