A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037907



Internal ID18780438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66975498..67173658hg38UCSC Ensembl
Innerchr10:68735256..68933416hg19UCSC Ensembl
Innerchr10:68405262..68603422hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38198161
hg19198161
hg18198161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv916n100
Supporting Variantsnssv3513130, nssv3509670
Samples
Known GenesCTNNA3, LRRTM3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037907
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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