A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053885



Internal ID18796416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:48314149..48346517hg38UCSC Ensembl
Innerchr15:48606346..48638714hg19UCSC Ensembl
Innerchr15:46393638..46426006hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3832369
hg1932369
hg1832369
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552377
Samples
Known GenesDUT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053885
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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