A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049754



Internal ID18792285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86604960..86699322hg38UCSC Ensembl
Innerchr10:88364717..88459079hg19UCSC Ensembl
Innerchr10:88354697..88449059hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3894363
hg1994363
hg1894363
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512210
Samples
Known GenesLDB3, OPN4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049754
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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