A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569065



Internal ID16009788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438557..34545691hg38UCSC Ensembl
Innerchr15:34730758..34837892hg19UCSC Ensembl
Innerchr15:32518050..32625184hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38107135
hg19107135
hg18107135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4476n54
Supporting Variantsnssv840231, nssv840233, nssv840234, nssv840229, nssv840232, nssv840230, nssv840225, nssv840237, nssv840228, nssv840226, nssv840224, nssv840236, nssv840235, nssv840227, nssv840223
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569065
Frequency
Sample Size17421
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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