A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567137



Internal ID16354546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19795973..19866420hg38UCSC Ensembl
Innerchr15:20001226..20071673hg19UCSC Ensembl
Innerchr15:18261234..18331687hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3870448
hg1970448
hg1870454
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv836868
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567137
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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