A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568810



Internal ID16009533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31483297..31484140hg38UCSC Ensembl
Innerchr15:31775500..31776343hg19UCSC Ensembl
Innerchr15:29562792..29563635hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38844
hg19844
hg18844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4435n54
Supporting Variantsnssv839601
Samples
Known GenesOTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568810
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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