A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611105



Internal ID16398514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40327353..40356310hg38UCSC Ensembl
Innerchr8:40184872..40213829hg19UCSC Ensembl
Innerchr8:40304029..40332986hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3828958
hg1928958
hg1828958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1111287
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611105
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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