A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045409



Internal ID19134628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113220500..113262682hg38UCSC Ensembl
Innerchr13:113874814..113916996hg19UCSC Ensembl
Innerchr13:112922815..112964997hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3842183
hg1942183
hg1842183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525620
Samples
Known GenesCUL4A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045409
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