A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569067



Internal ID16009790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438557..34552372hg38UCSC Ensembl
Innerchr15:34730758..34844573hg19UCSC Ensembl
Innerchr15:32518050..32631865hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38113816
hg19113816
hg18113816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4476n54
Supporting Variantsnssv840258, nssv840253, nssv840254, nssv840262, nssv840259, nssv840251, nssv840250, nssv840255, nssv840263, nssv840252, nssv840260, nssv840257, nssv840261, nssv840256
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)nsv569067
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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