A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569334



Internal ID16356743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:47786868..47915269hg38UCSC Ensembl
Innerchr15:48079065..48207466hg19UCSC Ensembl
Innerchr15:45866357..45994758hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38128402
hg19128402
hg18128402
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149596
SamplesHGDP00148
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569334
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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