A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569809



Internal ID16357218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69105686..69119630hg38UCSC Ensembl
Innerchr15:69398026..69411969hg19UCSC Ensembl
Innerchr15:67185080..67199023hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3813945
hg1913944
hg1813944
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844368
Samples
Known GenesMIR548H4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569809
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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