A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570511



Internal ID16357920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93413254..93426666hg38UCSC Ensembl
Innerchr15:93956483..93969895hg19UCSC Ensembl
Innerchr15:91757487..91770899hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3813413
hg1913413
hg1813413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848928
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570511
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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