A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569399



Internal ID16010122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50582767..51270001hg38UCSC Ensembl
Innerchr15:50874964..51562198hg19UCSC Ensembl
Innerchr15:48662256..49349490hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38687235
hg19687235
hg18687235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4526n54
Supporting Variantsnssv842975
Samples
Known GenesAP4E1, CYP19A1, DCAF13P3, MIR4713, SPPL2A, TNFAIP8L3, TRPM7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569399
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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