A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035151



Internal ID18777682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:49939399..50593714hg38UCSC Ensembl
Innerchr13:50513535..51167850hg19UCSC Ensembl
Innerchr13:49411536..50065851hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38654316
hg19654316
hg18654316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523456
Samples
Known GenesDLEU1, DLEU2, KCNRG, MIR15A, MIR16-1, MIR3613, ST13P4, TRIM13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035151
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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