A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569193



Internal ID16356602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:36233729..36294090hg38UCSC Ensembl
Innerchr15:36525930..36586291hg19UCSC Ensembl
Innerchr15:34313222..34373583hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3860362
hg1960362
hg1860362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv840693, nssv840694
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569193
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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