A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611545



Internal ID16398954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74452293..74454285hg38UCSC Ensembl
Innerchr8:75364528..75366520hg19UCSC Ensembl
Innerchr8:75527083..75529075hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381993
hg191993
hg181993
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12202n54
Supporting Variantsnssv1116181, nssv1116178, nssv1116182, nssv1116179, nssv1116176, nssv1116180, nssv1116174, nssv1116175, nssv1116177
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611545
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer