A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046759



Internal ID18789290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43057447..43096169hg38UCSC Ensembl
Innerchr10:43552895..43591617hg19UCSC Ensembl
Innerchr10:42872901..42911623hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3838723
hg1938723
hg1838723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv723n100
Supporting Variantsnssv3516784, nssv3522728, nssv3510217
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)nsv1046759
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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