A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051784



Internal ID18794315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101587705..101790849hg38UCSC Ensembl
Innerchr15:102127908..102331052hg19UCSC Ensembl
Innerchr15:99945431..100148575hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38203145
hg19203145
hg18203145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555376
Samples
Known GenesTARSL2, TM2D3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051784
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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