A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569228



Internal ID16009951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40814287..40901953hg38UCSC Ensembl
Innerchr15:41106485..41194151hg19UCSC Ensembl
Innerchr15:38893777..38981443hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3887667
hg1987667
hg1887667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842219
Samples
Known GenesPPP1R14D, RHOV, SPINT1, VPS18, ZFYVE19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569228
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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