A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550406



Internal ID15991129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35631696..35641744hg38UCSC Ensembl
Innerchr10:35920624..35930672hg19UCSC Ensembl
Innerchr10:35960630..35970678hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3810049
hg1910049
hg1810049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1035n54
Supporting Variantsnssv746840
Samples
Known GenesFZD8, MIR4683
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550406
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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