A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570449



Internal ID16357858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:91694565..91791526hg38UCSC Ensembl
Innerchr15:92237795..92334756hg19UCSC Ensembl
Innerchr15:90038799..90135760hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3896962
hg1996962
hg1896962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848582
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570449
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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