A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567328



Internal ID16354737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20340409..21002347hg38UCSC Ensembl
Innerchr15:20545662..21207676hg19UCSC Ensembl
Innerchr15:18805676..19472335hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38661939
hg19662015
hg18666660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4182n54
Supporting Variantsnssv837125
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)nsv567328
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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