A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569202



Internal ID16356611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37258871..37274560hg38UCSC Ensembl
Innerchr15:37551072..37566761hg19UCSC Ensembl
Innerchr15:35338364..35354053hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3815690
hg1915690
hg1815690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148857
SamplesHGDP00929
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569202
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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