A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568301



Internal ID16009024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23360531..23438636hg38UCSC Ensembl
Innerchr15:23605678..23683783hg19UCSC Ensembl
Innerchr15:21157119..21235224hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3878106
hg1978106
hg1878106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4332n54
Supporting Variantsnssv838447
Samples
Known GenesGOLGA8S
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568301
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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