A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051682



Internal ID18794213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43083220..43094310hg38UCSC Ensembl
Innerchr10:43578668..43589758hg19UCSC Ensembl
Innerchr10:42898674..42909764hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3811091
hg1911091
hg1811091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv727n100
Supporting Variantsnssv3515429, nssv3512736
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)nsv1051682
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