A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041228



Internal ID19130447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113505488..113539563hg38UCSC Ensembl
Innerchr13:114159803..114193878hg19UCSC Ensembl
Innerchr13:113207804..113241879hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3834076
hg1934076
hg1834076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525638
Samples
Known GenesTMCO3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041228
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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