A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611103



Internal ID16398512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40327353..40340695hg38UCSC Ensembl
Innerchr8:40184872..40198214hg19UCSC Ensembl
Innerchr8:40304029..40317371hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3813343
hg1913343
hg1813343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12116n54
Supporting Variantsnssv1111285
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611103
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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