A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570359



Internal ID16357768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87171817..87208615hg38UCSC Ensembl
Innerchr15:87715048..87751846hg19UCSC Ensembl
Innerchr15:85516052..85552850hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3836799
hg1936799
hg1836799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848134
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570359
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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