A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570899



Internal ID16011622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101495064..101733297hg38UCSC Ensembl
Innerchr15:102035267..102273500hg19UCSC Ensembl
Innerchr15:99852790..100091023hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38238234
hg19238234
hg18238234
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4792n54
Supporting Variantsnssv1149272
Samples1780862225_A
Known GenesTARSL2, TM2D3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570899
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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