A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570708



Internal ID16011431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98648638..98650295hg38UCSC Ensembl
Innerchr15:99191867..99193524hg19UCSC Ensembl
Innerchr15:97009390..97011047hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381658
hg191658
hg181658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4766n54
Supporting Variantsnssv849612, nssv849611
Samples
Known GenesIGF1R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570708
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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