A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569070



Internal ID16009793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438557..34689743hg38UCSC Ensembl
Innerchr15:34730758..34981944hg19UCSC Ensembl
Innerchr15:32518050..32769236hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38251187
hg19251187
hg18251187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4468n54
Supporting Variantsnssv840267
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)nsv569070
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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