A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567429



Internal ID16354838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380145..21000160hg38UCSC Ensembl
Innerchr15:20585398..21205489hg19UCSC Ensembl
Innerchr15:18845412..19470148hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38620016
hg19620092
hg18624737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4182n54
Supporting Variantsnssv837256
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)nsv567429
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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