A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568661



Internal ID16356070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27669419..27682695hg38UCSC Ensembl
Innerchr15:27914565..27927841hg19UCSC Ensembl
Innerchr15:25588160..25601436hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3813277
hg1913277
hg1813277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839288
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568661
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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