A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611550



Internal ID16398959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74452293..74456081hg38UCSC Ensembl
Innerchr8:75364528..75368316hg19UCSC Ensembl
Innerchr8:75527083..75530871hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg383789
hg193789
hg183789
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1116972, nssv1116963, nssv1116979, nssv1116970, nssv1116969, nssv1116976, nssv1116965, nssv1116973, nssv1116977, nssv1116967, nssv1116971, nssv1116980, nssv1116961, nssv1116978, nssv1116966, nssv1116964, nssv1116968, nssv1116975, nssv1116981, nssv1116974, nssv1116982, nssv1116959, nssv1116962, nssv1116960
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611550
Frequency
Sample Size17421
Observed Gain11
Observed Loss13
Observed Complex0
Frequencyn/a


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