A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570900



Internal ID16011623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101495064..101786434hg38UCSC Ensembl
Innerchr15:102035267..102326637hg19UCSC Ensembl
Innerchr15:99852790..100144160hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38291371
hg19291371
hg18291371
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4792n54
Supporting Variantsnssv851205
Samples
Known GenesTARSL2, TM2D3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570900
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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