A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569201



Internal ID16356610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37251359..37271672hg38UCSC Ensembl
Innerchr15:37543560..37563873hg19UCSC Ensembl
Innerchr15:35330852..35351165hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3820314
hg1920314
hg1820314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv840704
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569201
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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