A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039890



Internal ID18782421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43057447..43094310hg38UCSC Ensembl
Innerchr10:43552895..43589758hg19UCSC Ensembl
Innerchr10:42872901..42909764hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3836864
hg1936864
hg1836864
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv723n100
Supporting Variantsnssv3509649
Samples
Known GenesRET
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039890
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