A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567206



Internal ID16354615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20062612..21022154hg38UCSC Ensembl
Innerchr15:20267865..21227483hg19UCSC Ensembl
Innerchr15:18527879..19492142hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38959543
hg19959619
hg18964264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4164n54
Supporting Variantsnssv836955
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567206
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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