A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568969



Internal ID16009692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34413285..34560614hg38UCSC Ensembl
Innerchr15:34705486..34852815hg19UCSC Ensembl
Innerchr15:32492778..32640107hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38147330
hg19147330
hg18147330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4459n54
Supporting Variantsnssv839855
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568969
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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