A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569222



Internal ID16356631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:39287229..39306191hg38UCSC Ensembl
Innerchr15:39579430..39598392hg19UCSC Ensembl
Innerchr15:37366722..37385684hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3818963
hg1918963
hg1818963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv841133
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569222
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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