A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570903



Internal ID16011626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101505162..101733297hg38UCSC Ensembl
Innerchr15:102045365..102273500hg19UCSC Ensembl
Innerchr15:99862888..100091023hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38228136
hg19228136
hg18228136
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4792n54
Supporting Variantsnssv851209
Samples
Known GenesTARSL2, TM2D3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570903
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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