A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610067



Internal ID16050790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7418480..7945154hg38UCSC Ensembl
Innerchr8:7276002..7802676hg19UCSC Ensembl
Innerchr8:7263412..7840086hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38526675
hg19526675
hg18576675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11913n54
Supporting Variantsnssv1105765
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4A, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11A, SPAG11B, ZNF705B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610067
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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