A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570901



Internal ID16011624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101497780..101733297hg38UCSC Ensembl
Innerchr15:102037983..102273500hg19UCSC Ensembl
Innerchr15:99855506..100091023hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38235518
hg19235518
hg18235518
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4792n54
Supporting Variantsnssv851207, nssv851206
Samples
Known GenesTARSL2, TM2D3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570901
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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