A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567150



Internal ID16354559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20009274..22298543hg38UCSC Ensembl
Innerchr15:20214527..22586494hg19UCSC Ensembl
Innerchr15:18474541..20087858hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382289270
hg192371968
hg181613318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4162n54
Supporting Variantsnssv836883
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567150
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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