A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567319



Internal ID16354728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20300975..21053708hg38UCSC Ensembl
Innerchr15:20506228..21259037hg19UCSC Ensembl
Innerchr15:18766242..19523696hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38752734
hg19752810
hg18757455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4182n54
Supporting Variantsnssv837115
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)nsv567319
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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