A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567276



Internal ID16354685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20207597..21031548hg38UCSC Ensembl
Innerchr15:20412850..21236877hg19UCSC Ensembl
Innerchr15:18672864..19501536hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38823952
hg19824028
hg18828673
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4166n54
Supporting Variantsnssv837046
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)nsv567276
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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