A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611099



Internal ID16398508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40324784..40332421hg38UCSC Ensembl
Innerchr8:40182303..40189940hg19UCSC Ensembl
Innerchr8:40301460..40309097hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg387638
hg197638
hg187638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12114n54
Supporting Variantsnssv1111273, nssv1111272
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611099
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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