A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569813



Internal ID16357222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70183361..70198311hg38UCSC Ensembl
Innerchr15:70475700..70490650hg19UCSC Ensembl
Innerchr15:68262754..68277704hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3814951
hg1914951
hg1814951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149237
SamplesHGDP01163
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569813
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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