A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567448



Internal ID16354857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20384761..21110356hg38UCSC Ensembl
Innerchr15:20590014..21315685hg19UCSC Ensembl
Innerchr15:18850028..19580344hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38725596
hg19725672
hg18730317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4182n54
Supporting Variantsnssv837277
Samples
Known GenesCT60, 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)nsv567448
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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