A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611100



Internal ID16398509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40324784..40333357hg38UCSC Ensembl
Innerchr8:40182303..40190876hg19UCSC Ensembl
Innerchr8:40301460..40310033hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg388574
hg198574
hg188574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12114n54
Supporting Variantsnssv1111274
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611100
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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