A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049411



Internal ID19138630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66515307..66737409hg38UCSC Ensembl
Innerchr10:68275065..68497167hg19UCSC Ensembl
Innerchr10:67945071..68167173hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38222103
hg19222103
hg18222103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv902n100
Supporting Variantsnssv3515933
Samples
Known GenesCTNNA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049411
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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