A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611221



Internal ID16398630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45927486..45946058hg38UCSC Ensembl
Innerchr8:46839108..46857680hg19UCSC Ensembl
Innerchr8:46958273..46976845hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3818573
hg1918573
hg1818573
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12138n54
Supporting Variantsnssv1114107, nssv1114106, nssv1114101, nssv1114103, nssv1114105, nssv1114099, nssv1114100, nssv1114104, nssv1114102
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611221
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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