A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570908



Internal ID16011631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101683568..101737504hg38UCSC Ensembl
Innerchr15:102223771..102277707hg19UCSC Ensembl
Innerchr15:100041294..100095230hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3853937
hg1953937
hg1853937
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4800n54
Supporting Variantsnssv851213
Samples
Known GenesTARSL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570908
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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