A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569069



Internal ID16009792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438557..34679782hg38UCSC Ensembl
Innerchr15:34730758..34971983hg19UCSC Ensembl
Innerchr15:32518050..32759275hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38241226
hg19241226
hg18241226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4468n54
Supporting Variantsnssv840266
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2, MIR5588
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569069
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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