A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051400



Internal ID18793931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50598136..50754086hg38UCSC Ensembl
Innerchr15:50890333..51046283hg19UCSC Ensembl
Innerchr15:48677625..48833575hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38155951
hg19155951
hg18155951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552395
Samples
Known GenesSPPL2A, TRPM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051400
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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