A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567389



Internal ID16354798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20377197..20853331hg38UCSC Ensembl
Innerchr15:20582450..21058660hg19UCSC Ensembl
Innerchr15:18842464..19323248hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38476135
hg19476211
hg18480785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4183n54
Supporting Variantsnssv837192
Samples
Known GenesCXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, POTEB, POTEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567389
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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