A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569400



Internal ID16010123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50582767..51475068hg38UCSC Ensembl
Innerchr15:50874964..51767265hg19UCSC Ensembl
Innerchr15:48662256..49554557hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38892302
hg19892302
hg18892302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4526n54
Supporting Variantsnssv842976
Samples
Known GenesAP4E1, CYP19A1, DCAF13P3, DMXL2, GLDN, MIR4713, SPPL2A, TNFAIP8L3, TRPM7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569400
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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