A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049670



Internal ID18792201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43079488..43094310hg38UCSC Ensembl
Innerchr10:43574936..43589758hg19UCSC Ensembl
Innerchr10:42894942..42909764hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3814823
hg1914823
hg1814823
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv726n100
Supporting Variantsnssv3512122
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)nsv1049670
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