A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569090



Internal ID16009813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34444307..34690183hg38UCSC Ensembl
Innerchr15:34736508..34982384hg19UCSC Ensembl
Innerchr15:32523800..32769676hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38245877
hg19245877
hg18245877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4468n54
Supporting Variantsnssv840309
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)nsv569090
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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