A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567202



Internal ID16354611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20054126..21052895hg38UCSC Ensembl
Innerchr15:20259379..21258224hg19UCSC Ensembl
Innerchr15:18519393..19522883hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38998770
hg19998846
hg181003491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4164n54
Supporting Variantsnssv836951
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)nsv567202
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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